- combination of mFISH using human whole chromosome painting probes and the inverted DAPI-banding pattern

e.g.

- IPM-FISH: The resulting painting probes show a R-band like pattern concurrent to 24 M-FISH colors

• Aamot HV, Micci F, Holte H, Delabie J, Heim S (2005) G-banding and molecular cytogenetic analyses of marginal zone lymphoma. Br J Haematol 130:890-901
• Angle B, Yen F, Hersh JH, Gowans G, Barch M (2002) Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes. Am J Med Genet 111: 307-312.
• Borg I, Squire M, Menzel C, Stout K, Morgan D, Willatt L, O'Brien PC, Ferguson-Smith MA, Ropers HH, Tommerup N, Kalscheuer VM, Sargan DR (2002) A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation. J Med Genet 39:391-399.
• Corzo C, Petzold M, Mayol X, Espinet B, Salido M, Serrano S, Real FX, Sole F (2003) RxFISH karyotype and MYC amplification in the HT-29 colon adenocarcinoma cell line. Genes Chromosomes Cancer 36: 319-320.
• de Oliveira EH, Neusser M, Pieczarka JC, Nagamachi C, Sbalqueiro IJ, Muller S (2005) Phylogenetic inferences of Atelinae (Platyrrhini) based on multi-directional chromosome painting in Brachyteles arachnoides, Ateles paniscus paniscus and Ateles b. marginatus. Cytogenet Genome Res 108: 183-190.
• Durante M, George K, Cucinotta FA (2006) Chromosomes lacking telomeres are present in the progeny of human lymphocytes exposed to heavy ions. Radiat Res 165:51-58
• Espinet B, Salido M, Pujol RM, Florensa L, Gallardo F, Domingo A, Servitje O, Estrach T, Garcìa-Muret P, Woessner S, Serrano S, Solé F (2004) Genetic characterization of Sézary's syndrome by conventional cytogenetics and cross-species color banding fluorescent in situhybridization. Haematologica 89:165-173.
• Ferguson-Smith MA, Yang F, Rens W, O'Brien PC (2005) The impact of chromosome sorting and painting on the comparative analysis of primate genomes. Cytogenet Genome Res 108: 112-121.
• Harrison CJ, Gibbons B, Yang F, Butler T, Cheung KL, Kearney L, Dirscherl L, Bray-Ward P, Gregson M, Ferguson-Smith M (2000) Multiplex fluorescence in situ hybridization and cross species color banding of a case of chronic myeloid leukemia in blastic crisis with a complex Philadelphia translocation. Cancer Genet Cytogenet 116: 105-110.
• Harrison CJ, Yang F, Butler T, Cheung KL, O'Brien PC, Hennessy BJ, Prentice HG, Ferguson-Smith M (2001) Cross-species color banding in ten cases of myeloid malignancies with complex karyotypes. Genes Chromosomes Cancer 30: 15-24.
• Hills LV, Nouri S, Slater HR (2003) Pericentromeric euchromatin is conserved in minute human supernumerary chromosomes: a study using cross-species colour segmenting (RxFISH). Chromosome Res 11:359-363
• Hwang HJ, Kim GJ, Lee GB, Oh JT, Chun YH, Park SH (2003) A comprehensive karyotypic analysis on Korean hepatocellular carcinoma cell lines by cross-species color banding and comparative genomic hybridization. Cancer Genet Cytogenet 141: 128-137.
• Kim DG, Park SY, You KR, Lee GB, Kim H, Moon WS, Chun YH, Park SH (2001) Establishment and characterization of chromosomal aberrations in human cholangiocarcinoma cell lines by cross-species color banding. Genes Chromosomes Cancer 30: 48-56.
• Kim GJ, Park SY, Kim H, Chun YH, Park SH (2001) Chromosomal aberrations in neuroblastoma cell lines identified by cross species color banding and chromosome painting. Cancer Genet Cytogenet 129: 10-16.
• Koo SH, Kwon KC, Park JW, Lee YE, Kim JW (2000) Characterization of chromosomal breakpoints in an ALL patient using cross-species color banding. Cancer Genet Cytogenet 119: 118-120.
• Leite RP, Souto M, Carvalho B, Martins M, Chaves R, Morais A, Guedes-Pinto H, Wienberg J, Ribeiro E (2006) Identification, characterization and clinical implications of two markers detected at prenatal diagnosis. Prenat Diagn 26:920-924.
• Micci F, Teixeira MR, Dietrich CU, Saeter G, Bjerkehagen B, Heim S (1999) Combined RxFISH/G-banding allows refined karyotyping of solid tumors. Hum Genet 104: 370-375.
• Micci F, Teixeira MR, Heim S (2001) Complete cytogenetic characterization of the human breast cancer cell line MA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, and chromosome-specific painting. Cancer Genet Cytogenet. 131: 25-30.
• Micci F, Walter CU, Teixeira MR, Panagopoulos I, Bjerkehagen B, Saeter G, Heim S (2003) Cytogenetic and molecular genetic analyses of endometrial stromal sarcoma: nonrandom involvement of chromosome arms 6p and 7p and confirmation of JAZF1/JJAZ1 gene fusion in t(7;17). Cancer Genet Cytogenet 144: 119-124.
• Müller S, Neusser M, Wienberg J (2002) Towards unlimited colors for fluorescence in-situ hybridization (FISH). Chromosome Res 10: 223-232.
• Müller S, O'Brien PC, Ferguson-Smith MA, Wienberg J (1998) Cross-species colour segmenting: a novel tool in human karyotype analysis. Cytometry 33: 445-452.
• Müller S, Wienberg J (2000) Advances in the development of chromosome bar codes: Integration of M-FISH and Rx-FISH technology. medgen 12: 474-477 (German).
• Müller S, Wienberg J (2001) "Bar-coding" primate chromosomes: molecular cytogenetic screening for the ancestral hominoid karyotype. Hum Genet 109: 85-94.
• Neusser M, Munch M, Anzenberger G, Muller S (2005) Investigation of marmoset hybrids (Cebuella pygmaea x Callithrix jacchus) and related Callitrichinae (Platyrrhini) by cross-species chromosome painting and comparative genomic hybridization. Cytogenet Genome Res 108: 191-196.
• Park S-Y, Choi H-C, Chun Y-H, Kim H, Park S-H (2001) Characterization of chromosomal aberrations in lung cancer cell lines by cross-species color banding. Cancer Genet Cytogenet 124: 62-70.
• Pedrazzini E, Mamaev N, Yakovleva T, Sukhikh T, Salido M, Solé F, Prat E, Camps J, Miró R, Slavutsky I (2003) Genomic rearrangements involving rDNA and centromeric heterochromatin in vulvar epidermoid carcinoma cell line A-431. Cancer Genet Cytogenet 143:50-58
• Petek E, Wagner K, Steiner H, Schaffer H, Kroisel PM (2000) Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformation. Prenat Diagn 20: 349-352.
• Petek E, Windpassinger C, Vincent JB, Cheung J, Boright AP, Scherer SW, Kroisel PM, Wagner K (2001) Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome. Am J Hum Genet 68: 848-858.
• Salido M, Solé F, Espinet B, Zamora L, Woessner S, Florensa L (2001) New t(11;12)(q12;q11) characetrized by RxFISH in a patient with T-cell large granular lymphocyte leukemia. Cancer Genet Cytogenet 125: 70-73.
• Sanchez-Izquierdo D, Siebert R, Harder L, Marugan I, Gozzetti A, Price HP, Gesk S, Hernandez-Rivas JM, Benet I, Sole F, Sonoki T, LeBeau MM, Schlegelberger B, Dyer MJ, Garcia-Conde J, Martinez-Climent JA (2001) Detection of translocations affecting the BCL6 locus in B cell non-Hodgkin's lymphoma by interphase fluorescence in situ hybridization. Leukemia. 15: 1475-1484.
• Stanyon R, Bruening R, Stone G, Shearin A, Bigoni F (2005) Reciprocal painting between humans, De Brazza's and patas monkeys reveals a major bifurcation in the Cercopithecini phylogenetic tree. Cytogenet Genome Res 108: 175-182.
• Teixeira MR, Micci F, Dietrich CU, Heim S (1999) Cross-species color banding characterization of chromosomal rearrangements in leukemias with incomplete G-band karyotypes. Genes Chromosomes Cancer 26: 13-19.
• Teixeira MR, Micci F, Dietrich CU, Heim S (2000) Detailed genome-wide screening for inter- and intrachromosomal abnormalities by sequential G-banding and RxFISH color banding of the same metaphase cells. Cancer Genet Cytogenet 119: 94-101.
• Teixeira MR (2002) Combined classical and molecular cytogenetic analysis of cancer. Eur J Cancer 38: 1580-1584.
• Wienberg J (2005) Fluorescence in situ hybridization to chromosomes as a tool to understand human and primate genome evolution. Cytogenet Genome Res 108:139-160.
• Xue YB, Song X (2008) [Progresses on the methods of tumor chromosome aberration analysis.] Yi Chuan 30:1529-1535. Chinese.
• Zhao L, Hayes K, Glassman A (2000) Enhanced detection of chromosomal abnormalities with the use of RxFISH multicolor banding technique. Cancer Genet Cytogenet 118: 108-111.
• Zitzelsberger H, O'Brien B, Weier H-U (2002) Multicolor FISH techniques for the detection of inter- and intrachromosomal rearrangements. In: FISH-Technology, Springer-labmanual, Springer, Berlin, pp 408-424, ISBN: 3-540-67276-1.

This technique is based on band specific microdissection libraries and available for chromosomes 3 and 10 now.

• Kakazu N, Ashihara E, Hada S, Ueda T, Sasaki H, Terada M, See TA (2001) Development of spectral colour banding in cytogenetic analysis. Lancet 357: 529-530.
• Kakazu N, Bar-Am I, Hada S, Ago H, Abe T (2003) A new chromosome banding technique, spectral color banding (SCAN), for full characterization of chromosomal abnormalities. Genes Chromosomes Cancer 37: 412-416
• Kakazu N, Abe T (2006) Multicolor banding technique, spectral color banding (SCAN): new development and applications. Cytogenet Genome Res 114:250-256.
• Babu R, Van Dyke DL, Dev VG, Koduru P, Rao N, Mitter NS, Liu M, Fuentes E, Fuentes S, Papa S (2018) Interphase chromosome profiling: A method for conventional banded chromosome analysis using interphase nuclei. Arch Pathol Lab Med. 142:213-228.

This technique is based on changing fluorescence intensity ratios along the chromosomes, which are used to assign different pseudo-colours to specific chromosomal regions and allows the differentiation of chromosome region specific areas at the band and sub-band level. The MCB technique provides moreover the possibility to analyse chromosomes irrespective of their condensation grades.

• Aktas D, Weise A, Utine E, Alehan D, Mrasek K, Eggeling FV, Thieme H, Tuncbilek E, Liehr T (2009) Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report. Mol Cytogenet 2:14.
• Al Achkar W, Wafa A, Mkrtchyan H, Moassass F, Liehr T (2009) Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report. Mol Cytogenet 2:21.
• Al Achkar W, Wafa A, Mkrtchyan H, Moassas F, Liehr T (2010) A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3. Mol Cytogenet 3:6.
• Al Achkar W, Wafa A, Mkrtchyan H, Moassass F, Liehr T (2010) A unique complex translocation involving six different chromosomes in a case of childhood acute lymphoblastic leukemia with the Philadelphia chromosome and adverse prognosis. Oncol Lett 1:801-804.
• Al Achkar W, Wafa A, Ali BY, Manvelyan M, Liehr T (2010) A rare chronic myeloid leukemia case with Philadelphia chromosome, BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes. Oncol Lett 1:797-800.
• Al Achkar W, Wafa A, Mkrtchyan H, Moassass F, Liehr T (2010) A rare case of Philadelphia chromosome-positive chronic myelogenous leukemia with inversion in chromosome 9 and t(10;17). Oncol Lett 1:793-795.
• Al-Achkar W, Wafa A, Manvelyan M, Ikhtiar A, Liehr T (2010) De novo translocation involving two chromosomes in adult prolymphocytic leukemia--a rare case. Leuk Res 34:e345-347.
• Al-Achkar W, Wafa, Liehr T (2011) Complex translocation involving four chromosomes in a novel Philadelphia-positive chronic myeloid leukemia case. Onc Lett 2:273-276.
• Al Achkar W, Wafa A, Moassass F, Liehr T (2010) Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl. Mol Cytogenet 4;3:18.
• Al-Achkar W, Wafa A, Moassass F, Liehr (2012) A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12). Oncol Lett 3: 1027-1029.
• Al-Achkar W, Wafa A, Moassass F, Liehr T (2012) A unique cytogenetic abnormality, t(2;7)(p13.1;p21.3), in a Philadelphia-positive chronic myeloid leukemia. Onc Letters 4: 209-212.
• Al-Achkar W, Wafa A, Liehr T, Klein E, Moassass F (2012) Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype. Mol Med Report 6: 293-296.
• Al-Achkar W, Aljapawe A, Almedani S, Liehr T, Wafa A (2013) A novel cytogenetic abnormality t(7;8)(p11.2:q11.2) and a four-way Philadelphia translocation in an imatinib mesylate-resistant chronic myeloid leukemia patient. Oncol Lett 5: 617-620.
• Al-Achkar W, Wafa A, Liehr T (2013) A new t(9;11;20;22)(q34;p11.2;q11.21;q11) in a Philadelphia-positive chronic myeloid leukemia case. Oncol Lett 5: 605-608.
• Al-Achkar W, Wafa A, Moassass F, Klein E, Liehr T (2013) Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patient. Oncol Lett 5: 1579-1582.
• Al-Achkar W, Wafa A, Ikhtiar A, Liehr T (2013) Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate resistant chronic myeloid leukemia patient. Oncol Lett 5: 1656-1658.
• Al Achkar W, Wafa A, Aljapawe A, Liehr T (2013) A de novo del(9)(p22.3) in a primary plasma cell leukemia case. Mol Cytogenet, 6:33.
• Al-achkar W, Aljapawe A, Othman MA, Wafa A (2013) A de novo acute myeloid leukemia (AML-M4) case with a complex karyotype and yet unreported breakpoints. Molecular Cytogenetics 6:18.
• Al-Achkar W, Moassass F, Ikhtiar A, Othman MAK, Liehr T, Wafa A (2013) Cytogenetic evolution in a patient with chronic developing a secondary acute myelogenous leukemia subtype M5 resistant to Imatinib mesylate therapy. J Leuk 1: 118.
• Al Achkar W, Wafa A, Aljapawe A, Othman MAK, Liehr T (2013) A novel cytogenetic abnormality r(7)(::p11.2->q36.3::) in a Philadelphia-positive chronic myeloid leukemia case. Case Rep Clin Med 2: 517-520.
• Al-Achkar W, Wafa A, Othman MAK, Moassass F, Aljapawe A, Liehr T (2014) An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations. Mol Cytogenet 7: 60.
• Al-Achkar W, Moassass F, Al-Ablog A, Liehr T, Fan X, Wafa A (2015) A Syrian couple with chromosomal aberration and MTHFR polymorphism leads to recurrent pregnancy loss and partial trisomy of 5p12-15.3 in the offspring: Case report and review to the literature. Zhonghua Nan Ke Xue = Nat J Androl 21: 219-224.
• Alhalabi N, Al-Achkar W, Wafa A, Kenj M, Alhalabi M (2018) De novo balanced Robertsonian translocation rob(22;22)(q10;q10) in a woman with recurrent pregnancy loss: A rare case. J Reprod Infertil 19:61-66.
• Amasdl S, Natiq A, Elalaoui SC, Sbiti A, Liehr T, Sefiani A (2016) Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report. J Med Case Rep 10: 122
• Babicka L, Ransdorfova S, Brezinova J, Zemanova Z, Sindelarova L, Siskova M, Maaloufova J, Cermak J, Michalova K (2007) Analysis of complex chromosomal rearrangements in adult patients with MDS and AML by multicolor FISH. Leuk Res 31:39-47.
• Bakshi SR, Brahmbhatt MM, Trivedi PJ, Chudoba I (2006) Constitutional tetrasomy 18p. Indian Pediatr 43:357-360.
• Balci S, Engiz O, Aktas D, Vargel I, Beksac MS, Mrasek K, Vermeesch J, Liehr T (2006) Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies. Am J Med Genet A 140:628-632.
• Balci S, Unal A, Engiz O, Aktas D, Liehr T, Gross M, Mrasek K, Saygi S (2007) Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3). Dev Med Child Neurol 49:219-224.
• Balci S, Yuksel Konuk B, Atik F, Oguz AK, Ergun MA, Baltaci V, Kosyakova N, Liehr T (2010) Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouth. Genetic Counselling 21:317-324.
• Balikova I, Martens K, Melotte C, Amyere M, Van Vooren S, Moreau Y, Vetrie D, Fiegler H, Carter NP, Liehr T, Vikkula M, Matthijs G, Fryns JP, Casteels I, Devriendt K, Vermeesch JR (2008) Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16. Am J Hum Genet 82:181-187.
• Barber JC, Thomas NS, Collinson MN, Dennis NR, Liehr T, Weise A, Belitz B, Pfeiffer L, Kirchhoff M, Krag-Olsen B, Lundsteen C (2005) Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences. Eur J Hum Genet 13:283-291.
• Barber JC, Maloney V, Hollox EJ, Stuke-Sontheimer A, du Bois G, Daumiller E, Klein-Vogler U, Dufke A, Armour JA, Liehr T (2005) Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Eur J Hum Genet 13:1131-1136.
• Barber JC, Zhang S, Friend N, Collins AL, Maloney VK, Hastings R, Farren B, Barnicoat A, Polityko AD, Rumyantseva NV, Starke H, Ye S (2006) Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect. Cytogenet Genome Res 114:351-358.
• Barber JC, Hall V, Maloney VK, Huang S, Roberts AM, Brady AF, Foulds N, Bewes B, Volleth M, Liehr T, Mehnert K, Bateman M, White H (2013) 16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2. Eur J Hum Genet 21:182-189.
• Bartels I, Starke H, Argyriou L, Sauter SM, Zoll B, Liehr T (2007) An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype. Eur J Med Genet 50:133-138
• Behjati F, Shafaghati Y, Firouzabadi SG, Kahrizi K, Bagherizadeh I, Najmabadi H, Bint S, Ogilvie C. M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism. Eur J Med Genet 51:608-614.
• Benedek K, Chudoba I, Klein G, Wiener F, Mai S (2004) Rearrangements of the telomeric region of mouse chromosome 11 in Pre-B ABL/MYC cells revealed by mBANDing, spectral karyotyping, and fluorescence in-situ hybridization with a subtelomeric probe. Chromosome Res 12:777-785.
• Berardinelli F, De Vitis M, Nieri D, Cherubini R, De Nadal V, Gerardi S, Tanzarella C, Sgura A, Antoccia A (2015) mBAND and mFISH analysis of chromosomal aberrations and breakpoint distribution in chromosome 1 of AG01522 human fibroblasts that were exposed to radiation of different qualities. Mutat Res Genet Toxicol Environ Mutagen 793: 55-63.
• Bernardini L, Castori M, Capalbo A, Mokini V, Mingarelli R, Simi P, Bertuccelli A, Novelli A, Dallapiccola B (2007) Syndromic craniosynostosis due to complex chromosome 5 rearrangement and MSX2 gene triplication. Am J Med Genet A 143A:2937-2943.
• Bernardini L, Palka C, Ceccarini C, Capalbo A, Bottillo I, Mingarelli R, Novelli A, Dallapiccola B (2008) Complex rearrangement of chromosomes 7q21.13-q22.1 confirms the ectrodactyly-deafness locus and suggests new candidate genes. Am J Med Genet A 146A:238-244.
• Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Lefort G, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F (2007) Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Mol Hum Reprod 13:751-756.
• Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Manvelyan M, Hunstig F, Lefort G, Weise A, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F (2009) Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. Eur J Hum Genet 17:44-50.
• Bocian E, Nowakowska B, Obersztyn E, Borg K, Chudoba I, Kostyk E, Kruczek A, Pietrzyk J, Mazurczak T (2006) [Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations] Med Wieku Rozwoj 10(1 Pt 2):211-25. Polish.
• Borges ML, Capela de Matos RR, Amaral BD, Soares-Ventura EM, Leite EP, Silva MO, Cornélio MT, Silva ML, Liehr T, Marques-Salles T (2017) Molecular cytogenetic approach to characterize novel and cryptic chromosome abnormalities in childhood myeloid malignances of Fanconi anemia. J Ped Hematol Oncol 39: e85-e91.
• Brezinová J, Zemanová Z, Ransdorfová S, Pavlistová L, Babická L, Housková L, Melichercíková J, Sisková M, Cermák J, Michalová K (2007) Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies. Cancer Genet Cytogenet 173:10-16.
• Burégio-Frota P, Valença L, Leal GF, Duarte AR, Bispo-Brito AV, Soares-Ventura EM, Marques-Salles TJ, Nogueira MT, Muniz MT, Silva ML, Hunstig F, Liehr T, Santos N (2010) Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndrome. Genet Mol Res 9:780-784.
• Bystřická D, Zemanová Z, Březinová J, Gančarčíková M, Grosová L, Sárová I, Izáková S, Berková A, Michalová K (2010) The assessment of array comparative genomic hybridization in complex karyotype analyses. Folia Biol (Praha) 56:223-230.
• Callier P, Faivre L, Marle N, Thauvin-Robinet C, Sanlaville D, Gosset P, Prieur M, Labenne M, Huet F, Mugneret F (2006) Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterization. Am J Med Genet A 140:1859-1863.
• Carreira IM, Mascarenhas A, Matoso E, Couceiro AB, Ramos L, Dufke A, Mazauric M, Stressig R, Kosyakova N, Melo JB, Liehr T (2007) Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18. J Histochem Cytochem 55:1123-1128.
• Capela de Matos RR, De Figueiredo AF, Liehr T, Alhourani E, De Souza MT, Abdelhay, E Ribeiro RC, Silva MLM (2015) A novel three-way variant t(8;13;21)(q22;q33;q22) in a child with acute myeloid leukemia FAB AML-M2: contribution of molecular approaches to reveal t(8;21) variants. Acta Hematol 134: 243-245.
• Capela de Matos RR, Ney Garcia DR, Cifoni E, Othman MAK, Tavares de Souza M, Carboni EK, Ferreira GM, Liehr T, Ribeiro RC, M Silva (2017) MLGAS6 oncogene and reverse MLLT3-KMT2A duplications in an infant with acute myeloid leukemia and a novel complex hyperdiploid karyotype: detailed high-resolution molecular cytogenetic studies. Cytogenet Genome Res 152: 33-37.
• Castillo Taucher S, Fuentes AM, Paulos A, Pardo A (2002) [Multiple FISH and multiple BAND: Application of cytogenetic and molecular techniques in 5 cases] Rev Med Chil 130:511-518. Spanish
• Chae H, Kim M, Lim J, Kim Y, Han K, Lee S (2010) B lymphoblastic leukemia with ETV6 amplification. Cancer Genet Cytogenet 203:284-287.
• Cavdarli B, Ozgen G, Kaymak AO, Göker B, Liehr T, Ergun MA, Percin EF (2013) A case with double translocation and Sjögren syndrome. Turkiye Klinikleri J Med Sci 33:263-236.
• Chen CP, Chen M, Chern SR, Wu PS, Chang SP, Lee DJ, Chen YT, Chen LF, Su JW, Hwa-Ruey Hsieh A, Hwa-Jiun Hsieh A, Wang W (2012) Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2. Taiwan J Obstet Gynecol 51:411-417.
• Christofolini DM, Yoshimoto M, Squire JA, Brunoni D, Melaragno MI, Carvalheira G (2006) Hydrocephaly, penoscrotal transposition, and digital anomalies associated with de novo pseudodicentric rearranged chromosome 13 characterized by classical cytogenetic methods and mBAND analysis. Am J Med Genet A 140:1321-1325.
• Chudoba I, Senger G, Plesch A, Claussen U (1999) New developments in clinical cytogenetics. ECA Newsletter 3: 3-8.
• Chudoba I, Plesch A, Lorch T, Lemke J, Claussen U, Senger G (1999) High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes. Cytogenet Cell Genet, 84:156-160.
• Chudoba I, Senger G (2002) Microdissection of chromosomes and reverse FISH. In: FISH-Technology, Springer-labmanual, Springer, Berlin, pp 388-407, ISBN: 3-540-67276-1.
• Chudoba I, Hickmann G, Friedrich T, Jauch A, Kozlowski P, Senger G (2004) mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations. Cytogenet Genome Res 104:390-393
• Debiec-Rychter M, Marynen P, Hagemeijer A, Pauwels P (2003) ALK-ATIC fusion in urinary bladder inflammatory myofibroblastic tumor. Genes Chromosomes Cancer 38:187-190.
• de Figueiredo AF, Liehr T, Bhatt S, Binato R, Soares Ventura EM, de Souza MT, Rodrigues Capela de Matos R, Correa Ribeiro R, Abdelhay E, Macedo Silva ML (2010) A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5. Blood Cells Mol Dis 2010, 45:197-198
• de Figueiredo AF, Capela de Matos RR, Othman MA, Liehr T, da Costa ES, Land MG, Ribeiro RC, Abdelhay E, Silva ML (2015) Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia. Mol Cytogenet 8: 62.
• de Jesus Marques-Salles T, Liehr T, Mkrtchyan H, Raimondi SC, Tavares de Souza M, Faria de Figueiredo A, Rouxinol S, Jordy Macedo FC, Abdelhay E, Santos N, Macedo Silva ML (2009) A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia. Cancer Genet Cytogenet 189:59-62
• de Jesus Marques-Salles T, da Silva Barros JEX, Soares-Ventura EM, Cartaxo-Muniz MT, Santos N, Ferreira E, Macedo Silva ML, Liehr T, Mkrtchyan H (2010) Unusual childhood biphenotypic acute leukemia with a yet unreported t(3;13)(p25.1;q13). Leuk Res 34: e206-e207.
• de Souza M, Hassan R, Liehr T, Marques-Salles T, Boulhosa AM, Abdelhay E, Ribeiro R, Silva MLM (2014) Conventional and molecular cytogenetic characterization of Burkitt lymphoma with bone marrow involvement in Brazilian children and adolescents. Ped Blood Cancer 61: 1422-1426.
• de Souza DC, de Figueiredo AF, Ney Garcia DR, da Costa ES, Othman MAK, Liehr T, Abdelhay E, Silva MLM, de Souza Fernandez T (2017) A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome. Mol Cytogenet 10: 35.
• de Souza MT, Vera-Lozada G, Othman M, Marques-Salles TJ, Pinto LW, da Rocha MM, Rouxinol S, Liehr T, Ribeiro RC, Hassan R, Silva MLM (2018) Molecular and cytogenetic studies in a child with Burkitt lymphoma and ataxia-telangiectasia syndrome harboring MYC overexpression and partial trisomy 8. Ann Lab Med 38: 63-66.
• Douet-Guilbert N, Basinko A, Eveillard JR, Morel F, Le Bris MJ, Guéganic N, Bovo C, Herry A, Berthou C, De Braekeleer M (2010) Three rearrangements of chromosome 5 in a patient with myelodysplastic syndrome: an atypical deletion 5q, a complex intrachromosomal rearrangement of chromosome 5, and a paracentric inversion of chromosome 5. Cancer Genet Cytogenet 203:303-308.
• Dufke A, Walczak C, Liehr T, Starke H, Trifonov V, Rubtsov N, Schöning M, Enders H, Eggermann T (2001) Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, iverted duplicated marker. Europ J Hum Genet, 9:572-576.
• Dufke A, Singer S, Borell-Kost S, Stotter M, Pflumm DA, Mau-Holzmann UA, Starke H, Mrasek K, Enders H (2006) De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies. Cytogenet Genome Res 114:342-350.
• Egritas O, Cavdarli B, Dalgic B, Ergun MA, Percin F, Ziegler M, Pohle B, Liehr T (2010) Duplication 4q associated with chronic cholestatic changes in liver biopsy. Eur J Med Genet;53:411-414.
• Ergul E, Liehr T, Mrasek K, Sazci A (2009) A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male. Fertil Steril 92:391.e9-391.e12.
• Fan X, Pinthong K, Mkrtchyan H, Siripiyasing P, Kosyakova N, Supiwong W, Tanomtong A, Chaveerach A, Liehr T, de Bello Cioffi M, Weise A (2013) First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae). Mol Cytogenet 6:58.
• Fan X, Pinthong K, Mkrtchyan H, Siripiyasing P, Kosyakova N, Supiwong W, Tanomtong A, Chaveerach A, Liehr T, de Bello Cioffi M, Weise A (2013) First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae). Mol Cytogenet 6:58.
• Fan X, Sangpakdee W, Tanomtong A, Chaveerach A, Pinthong K, Pornnarong S, Supiwong W, Trifonov VA, Hovhannisyan GG, Aroutouinian RM, Liehr T, Weise A (2014) Molecular cytogenetic analysis of Thai southern pig-tailed macaque (Macaca nemestrina) by multicolor banding. Proceedings of Yerevan State University 2014:46-50.
• Fan X, Tanomtong A, Chaveerach A, Pinthong K, Pornnarong S, Supiwong W, Liehr T, Weise A (2014) High resolution karyotype of Thai crab-eating macaque (Macaca fascicularis). Genetika 46: 877-882.
• Fan X, Sangpakdee W, Tanomtong A, Chaveerach A, Pinthong K, Pornnarong S, Supiwong W, Trifonov V, Hovhannisyan G, Loth K, Hensel C, Liehr T, Weise A (2014) Comprehensive molecular cytogenetic analysis of Barbary macaque (Macaca sylvanus). Biol J Arm 66:98-102.
• Fan X , Supiwong W, Weise A, Mrasek K, Kosyakova N, Tanomtong A, Pinthong K, Trifonov VA, de Bello Cioffi M, Grothmann P, Liehr T, de Oliveira EHC (2015) Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens. Helyion 1:e00042
• Faria De Figueiredo A, Liehr T, Bhatt S, Binato R, Tavares De Souza M, Rodrigues Capela De Matos R, De Jesus Marques Salles T, Jordy FC, Ribeiro RC, Abdelhay E, Luiza Macedo Silva M (2011) A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia. Leuk Lymphoma 52:1593-1596.
• Faria de Figueiredo A, Vieira TP, Liehr T, Bhatt S, Binato R, de Jesus Marques Salles T, Carboni E, Ribeiro RC, Macedo Silva ML, Abdelhay E (2012) A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5). Leuk Res 36: e74-e77.
• Fonzar Hernandes MA, de Jesus Marques-Salles T, Mkrtchyan H, Soares-Ventura EM, Pereira Leite E, Cartaxo Muniz MT, Marquim Nogueira Cornélio MT, Liehr T, Santos N, Macedo Silva ML. Extra copies of der(21)t(12;21) plus deletion of ETV6 gene due to dic(12;18) in B-cell precursor ALL with poor outcome. Case Reports Genet, 2012, doi: 10.1155/2012/186532
• Gazzo S, Chudoba I, Traverse-Glehen A, Baseggio L, Felman P, Berger F, Salles G, Hayette S, Magaud JP, Callet-Bauchu E (2007) Detailed characterization of 7q deletions by multicolor banding (mBAND) in marginal zone cell lymphoma. Cancer Genet Cytogenet 175:159-165.
• Gerdes AM, Hansen LK, Brandrup F, Soegaard K, Christoffersen A, Rasmussen K (2006) Pallister-Killian syndrome: Multiband FISH of tetrasomy 12p. Pediatr Dermatol. 2006 Jul-Aug;23(4):378-381.
• Gersak K, Writzl K, Veble A, Liehr T (2010) Primary amenorrhoea in a patient with mosaicism for monosomy X and a derivative X-chromosome. Genet Couns. 2010;21(3):335-342.
• Glaser M, Karst C, Gross M, Mkrtchyan H, Liehr T (2005) Chromosome torsions in cytogenetic preparations of bone-marrow - artifacts or leukemia-specific? Balk J Med Gen 8: 27-31.
• Grasshoff U, Singer S, Liehr T, Starke H, Fode B, Schoning M, Dufke A. (2003) A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q24-->1q22 and partial monosomy 4q27-->q28. Cytogenet Genome Res 103:17-23.
• Gross M, Starke H, Trifonov V, Claussen U, Liehr T, Weise A (2006) A molecular cytogenetic study of chromosome evolution in chimpanzee. Cytogenet Genome Res 112: 67-75.
• Gross M, Mkrtchyan H, Glaser M, Fricke HJ, Höffken K, Heller A, Weise A, Liehr T (2009) Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype. Int J Oncol 34:417-423.
• Guilherme RS, Dutra ARN, Perez AB, Takeno SS, Oliveira MM, Kulikowski D, Klein E, Hamid AB, Liehr T, Melaragno MI (2013) First report of a small supernumerary der(8;14) marker chromosome. Cytogenet Genome Res 139:284-288.
• Guilherme RS, Klein E, Hamid AB, Bhatt S, Volleth M, Polityko A, Kulpanovich A, Dufke A, Albrecht B, Morlot S, Brecevic L, Petersen MB, Manolakos E, Kosyakova N, Liehr T (2013) Human ring chromosomes - new insights for their clinical significance. Balk J Med Genet 16:13-19.
• Guilherme RS, Cernach MC, Sfakianakis TE, Takeno SS, Nardozza LM, Rossi C, Bhatt SS, Liehr T, Melaragno MI (2013) A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification. Cytogenet Genome Res 141:317-323.
• Hada M, Meador JA, Cucinotta FA, Gonda SR, Wu H (2007) Chromosome aberrations induced by dual exposure of protons and iron ions. Radiat Environ Biophys 46:125-129.
• Hada M, Cucinotta FA, Gonda SR, Wu H (2007) mBAND analysis of chromosomal aberrations in human epithelial cells exposed to low- and high-LET radiation. Radiat Res 168:98-105.
• Hada M, Gersey B, Saganti PB, Wilkins R, Cucinotta FA, Wu H (2010) mBAND analysis of chromosome aberrations in human epithelial cells induced by gamma-rays and secondary neutrons of low dose rate. Mutat Res 701:67-74.
• Hada M, Zhang Y, Feiveson A, Cucinotta FA, Wu H (2011) Association of inter- and intrachromosomal exchanges with the distribution of low- and high-LET radiation-induced breaks in chromosomes. Radiat Res 176:25-37.
• Hada M, Wu H, Cucinotta FA (2011) mBAND analysis for high- and low-LET radiation-induced chromosome aberrations: a review. Mutat Res 711:187-192.
• Hande MP, Azizova TV, Geard CR, Burak LE, Mitchell CR, Khokhryakov VF, Vasilenko EK, Brenner DJ (2003) Past exposure to densely ionizing radiation leaves a unique permanent signature in the genome. Am J Hum Genet 72: 1162-1170.
• Heller A, Starke H, Trifonov V, Rubtsov N, Wedding U, Loncarevic I, Bleck C, Claussen U, Liehr T (2002) A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML - characterization of the aberration by multicolor banding (MCB). In J Onc, Vol. 20, pp 1179-1181.
• Heller A, Trifonov V, Rubtsov N, Sauerbrey A, Starke H, Loncarevic IF, Claussen U, Liehr T. (2003) Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS. Oncol Reports, 10: 1789-1792.
• Heller A, Brecevic L, Glaser M, Loncarevic I, Gebhart E, Claussen U, Liehr T (2003) Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations. Cancer Genet Cytogenet 146:81-3.
• Heller A, Loncarevic IF, Glaser M, Gebhart E, Trautmann U, Claussen U, Liehr T (2004) Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints. Int J Oncol 24:127-36.
• Heller A, Fricke HJ, Starke H, Loncarevic IF, Claussen U, Liehr T (2004) Characterization of a highly aberrant plasma cell leukemia karyotype: a case report. Oncol Rep 11:89-92.
• Horstmann M, Obe G (2003) CABAND: Classification of aberrations in multicolor banded chromosomes. Cytogenet Genome Res 103:24-7.
• Hortsmann M, Durante M, Johannes C, Obe G (2005) Chromosomal intrachanges induced by swift iron ions. Adv Space Res 35:276-279.
• Houge G, Liehr T, Schoumans J, Ness GO, Solland K, Starke H, Claussen U, Stromme P, Akre B, Vermeulen S (2003) Ten years follow up of a boy with a complex chromosomal rearrangement: Going from a > 5 to 15-breakpoint CCR. Am J Med Genet 118A: 235-240.
• Hu J, Sathanoori M, Kochmar SJ, Surti U (2006) Application of multicolor banding for identification of complex chromosome 18 rearrangements. J Mol Diagn 8:521-525; quiz 528.
• Hu B, Grabham P, Nie J, Balajee AS, Zhou H, Hei TK, Geard CR (2012) Intrachromosomal changes and genomic instability in site-specific microbeam-irradiated and bystander human-hamster hybrid cells. Radiat Res 177:25-34.
• Iourov IY, Liehr T, Vorsanova SG, Kolotii AD, Yurov YB (2006) Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB). Chromosome Res 14: 223-229.
• Iourov IY, Liehr T, Vorsanova SG, Yurov YB (2007) Interphase chromosome-specific multicolor banding (ICS-MCB): a new tool for analysis of interphase chromosomes in their integrity. Biomol Eng 24:415-417.
• Iourov IY, Vorsanova SG, Liehr T, Monakhov VV, Soloviev IV, Yurov YB (2008) Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia. Cytogenet Genome Res 121:302-306.
• Iourov IY, Vorsanova SG, Liehr T, Yurov YB (2009) Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning. Neurobiology of Disease 2009; 34:212-220.
• Iourov IY, Vorsanova SG, Liehr T, Kolotii AD, Yurov YB (2009) Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain. Hum Mol Genet 18:2656-2669.
• Iourov IY, Liehr T, Vorsanova SG, Yurov YB. Interphase chromosome-specific multicolor banding. In: Human Interphase Chromosomes - Biomedical Aspects. Edited by Y.B. Yurov, S.G. Vorsanova, I.Y. Iourov, Springer, 2013, pp161-169.
• Jancuskova T, Plachy R, Stika J, Zemankova L, Hardekopf DW, Liehr T, Kosyakova N, Cmejla R, Zejskova L, Kozak T, Zak P, Zavrelova A, Havlikova P, Karas M, Junge A, Ramel C, Pekova S (2013) A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients. Leuk Res 37:1363-1373.
• Jarosova M, Holzerova M, Mihal V, Lakoma I, Divoky V, Blazek B, Pospisilova D, Hajduch M, Novak Z, Dusek L, Koptikova J, Poulsen TS, Indrak K (2003) Complex karyotypes in childhood acute lymphoblastic leukemia: cytogenetic and molecular cytogenetic study of 21 cases. Cancer Genet Cytogenet 145: 161-168.
• Johannes C, Chudoba I, Obe G (1999) Analysis of X-ray-induced aberrations in human chromosome 5 using high-resolution multicolour banding FISH (mBAND). Chromosome Res 7: 625-633.
• Johannes C, Horstmann M, Durante M, Chudoba I, Obe G (2004) Chromosome intrachanges and interchanges detected by multicolor banding in lymphocytes: searching for clastogen signatures in the human genome. Radiat Res 161:540-548.
• Karadeniz N, Mrasek K, Weise A (2008) Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding. Mol Cytogenet 1:17.
• Karadeniz N, Liehr T, Mrasek K, Aşık I, Aşık Z, Kosyakova N, Mkrtchyan H (2013) C-type lectins and human epithelial membrane protein1: Are they new proteins in keratin disorders? Open J Genet 3:262-269.
• Karst C, Heller A, Claussen U, Gebhart E, Liehr T (2005) Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia. Int J Oncol 27: 355-359.
• Karst C, Gross M, Haase D, Wedding U, Höffken K, Liehr T, Mkrtchyan H (2006) Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches. Int J Oncol 28:891-897.  
• Kautenburger T, Beyer-Sehlmeyer G, Festag G, Haag N, Kühler S, Küchler A, Weise A, Marian B, Peters WH, Liehr T, Claussen U, Pool-Zobel BL (2005) The gut fermentation product butyrate, a chemopreventive agent, suppresses glutathione S-transferase theta (hGSTT1) and cell growth more in human colon adenoma (LT97) than tumor (HT29) cells. J Cancer Res Clin Oncol 131:692-700.
• Kjeldsen E (2018) A novel acquired t(2;4)(q36.1;q24) with a concurrent submicroscopic del(4)(q23q24) in an adult with polycythemia vera. Cancers (Basel) 10: E214.
  
• Klein E, Manvelyan M, Simonyan I, Hamid AB, Santos Guilherme R, Liehr T, Karamysheva T (2012) Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics. Mol Cytogenet 5:15.
• Klein E, Rocchi M, Ovens-Raeder A, Kosyakova N, Weise A, Ziegler M, Meins M, Morlot S, Fischer W, Volleth M, Polityko A, Mackie Ogilvie C, Kraus C, Liehr T (2012) Five novel locations of neocentromeres in human: 18q22.1, Xq27.1~27.2, acro p13, acro p12, and heterochromatin of unknown origin. Cytogenet Genome Res 136:163-166.
• Kline AD, Griffin CA, Haddadin MH, Chudoba I, Morsberger LA, Hawkins AL, Amato RS, Munshi G, Cohen MM (2004) A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies. Am J Med Genet 129A:124-129.
• Koç A, Kan D, Karaer K, Ergün MA, Karaoğuz MY, Gücüyener K, Hinreiner S, Liehr T, Perçin EF (2008) An unexpected finding in a child with neurological problems: mosaic ring chromosome 18. Eur J Pediatr 167:655-659.
• Kosyakova N, Weise A, Mrasek K, Claussen U, Liehr T, Nelle H (2009) The hierarchically organized splitting of chromosomal bands for all human chromosomes. Mol Cytogenet 2:4
• Kuechler A, Weise A, Michel S, Schaeferhenrich A, Pool-Zobel PL, Claussen U, Liehr T (2003) Precise breakpoint characterization of the colon adenocarcinoma cell line HT-29 clone 19A by means of 24-color fluorescence in situ hybridization and multicolor banding. Genes Chr Cancer, 36:207-210.
• Kuechler A, Ziegler M, Blank C, Rommel B, Bullerdiek J, Ahrens J, Claussen U, Liehr T (2005) A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection. J Histochem Cytochem 53:355-357.
• Kyriazoglou AI, Rizou H, Dimitriadis E, Arnogiannaki N, Agnantis N, Pandis N (2013) Cytogenetic analysis of a low-grade secondary peripheral chondrosarcoma arising in synovial chondromatosis. In Vivo 27:57-60.
• Landais E, Leroy C, Kleinfinger P, Brunet S, Koubi V, Pietrement C, Poli-Mérol ML, Fiquet C, Souchon PF, Beri M, Jonveaux P, Garnotel R, Gaillard D, Doco-Fenzy M (2015) A pure familial 6q15q21 split duplication associated with obesity and transmitted with partial reduction. Am J Med Genet A 167:1275-1284.
  
• Leach NT, Chudoba I, Stewart TV, Holmes LB, Weremowicz S (2007) Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver-Russell syndrome. Am J Med Genet A 143A:1489-1493.
• Lee NC, Chang SP, Chang CS, Chen CH, Lee DJ, Lin CC, Hwu WL, Chen M (2009) Cryptic subtelomeric deletion plus inverted duplication at chromosome 18q in a fetus: molecular delineation by multicolor banding. Prenat Diagn 29:1058-1060.
• Lee NC, Chen M, Ma GC, Lee DJ, Wang TJ, Ke YY, Chien YH, Hwu WL (2010) Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints. Am J Med Genet A 152A:2327-2334.
• Ledig S, Preisler-Adams S, Morlot S, Liehr T, Wieacker P (2015) Premature ovarian failure caused by a heterozygous missense mutation in POF1B and a reciprocal translocation 46,X,t(X;3)(q21.1;q21.3). Sex Dev 9: 86-90.
• Lehrer H, Weise A, Michel S, Starke H, Mrasek K, Heller A, Kuechler A, Claussen U, Liehr T (2004) The hierarchically organized splitting of chromosomal bands into sub-bands analyzed by multicolor banding (MCB). Cytogenet Genome Res 105:25-28.
• Lemke J, Chudoba I, Senger G, Stumm M, Loncarevic IF, Henry C, Zabel B, Claussen U (2001) Improved definition of chromosomal breakpoints using high resolution multicolour banding (MCB). Hum Genet 108: 478-483.
• Lemke J, Claussen J, Michel S, Chudoba I, Mühlig P, Westermann M, Sperling K, Rubtsov N, Grummt UW, Ullmann P, Kromeyer-Hauschild K, Liehr T, Claussen U (2002) The DNA-based structure of human chromosome 5 in interphase. Am J Hum Genet 71: 1051-1059.
• Lestou VS, Gascoyne RD, Salski C, Connors JM, Horsman DE (2002) Uncovering novel inter- and intrachromosomal chromosome 1 aberrations in follicular lymphomas by using an innovative multicolor banding technique. Genes Chromosomes Cancer, 34: 201-210.
• Lestou VS, O’Connel JX, Ludkovski O, Gosling H, Lesack D, Horsmann DE (2002) Coamplification of 12p11 and 12q13~q22 in multiple ring chromosomes in a spindle cell sarcoma resolved by novel multicolor fluorescence in situ hybridization analysis. Cancer Genet Cytogenet 139: 44-47.
• Lestou VS, Ludkovski O, Connors JM, Gascoyne RD, Lam WL, Horsman DE (2003) Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis. Genes Chromosomes Cancer 36: 375-381.
• Liehr T (2008) Multicolor-fluorescence in situ hybridization. molecular cytogenetics in current diagnostics and research. Medgen 20: 374-378 (German)
• Liehr T, Heller A, Starke H, Rubtsov N, Trifonov V, Mrasek K, Weise A, Kuechler A, Claussen U (2002) Microdissection based high resolution multicolor banding for all 24 human chromosomes. Int J Mol Med, 9: 335-339.
• Liehr T, Schmidt M, Starke H, Ziegler M, Kittner G, Heller A, Rubtsov N, Trifonov V, Claussen U (2002) First case of trisomy 13 plus mosaic trisomy 1q. Fet Diag Ther, 17: 133-136.
• Liehr T, Claussen U (2002) Review: Multicolor-FISH approaches for the characterization of human chromosomes in clinical genetics and tumor cytogenetics. Current Genomics 3: 213-235.
• Liehr T, Weise A, Heller A, H Starke, Mrasek K, Kuechler A, Weier H-UG , Claussen U. Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries. Cytogenet Genome Res, 97: 43-47.
• Liehr T, Nietzel A, Starke H, Heller A, Weise A, Kuechler A, Senger G, Ebner S, Martin T, Stumm M, Wegner R, Tönnies H, Hoppe C, Claussen U, von Eggeling F (2003) Characterization of small marker chromosomes (SMC) by recently developed molecular cytogenetic approaches. J Ass Genet Techn 29: 5-10.
• Liehr T, Starke H, Heller A, Weise A, Beensen V, Senger G, Kittner G, Prechtel M, Claussen U, Seidel J (2003) Evidence for a new microdeletion syndrome in 15q21. Int J Mol Med 11: 575-578.
• Liehr T, Heller A, Eichhorn KH, Beensen V, Schulze E, Starke H, Claussen U, Schreyer I. (2004) Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2). Prenat Diagn 24:1022-1024.
• Liehr T, Gross M, Karst C, Glaser M, Mrasek K, Starke H, Weise A, Mkrtchyan H, Kuechler A (2006) FISH banding in tumor cytogenetics. Cancer Genet Cytogenet 164:88-89.
• Liehr T, Starke H, Heller A, Kosyakova N, Mrasek K, Gross M, Karst C, Steinhaeuser U, Hunstig F, Fickelscher I, Kuechler A, Trifonov V, Romanenko SA, Weise A (2006) Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding. Cytogenet Genome Res 114: 240-244.
• Liehr T, Utine GE, Trautmann U, Rauch A, Kuechler A, Pietracz J, Bocian E, Kosyakova N, Mrasek K, Boduroglu K, Weise A, Aktas D (2007) Neocentric small supernumerary marker chromosomes (sSMC) - three more cases plus review of the literature. Cytogenet Genome Res 118: 31-37.
• Liehr T, Kosyakova N, Weise A, Ziegler M, Raabe-Meyer G (2009) First case of a neocentromere formation in an otherwise normal chromosome 7. Cytogenet Genome Res 2010, 218: 189-191.
• Liehr T, Weise A, Hinreiner S, Mkrtchyan H, Mrasek K, Kosyakova N (2010) Characterization of chromosomal rearrangements using multicolor-banding (MCB/m-band). Methods Mol Biol 659:231-238.
• Liehr T, Kosayakova N, Schröder J, Ziegler M, Kreskowski K, Pohle B, Bhatt S, Theuss L, Wilhelm K, Weise A, Mrasek A. Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements. Balk J Med Genet 2011, 14:13-16.
• Liehr T, Mkrtchyan H, Manvelyan M, Karamysheva T, Klein E, Bhatt S. Chromosome architecture studied by high-resolution FISH-banding in three dimensionally preserved human interphase nuclei. In: Human Interphase Chromosomes - Biomedical Aspects. Edited by Y.B. Yurov, S.G. Vorsanova, I.Y. Iourov, Springer, 2013, pp171-178.
• Liehr T, Weise A, Hamid AB, Fan X, Klein E, Aust N, Othman MA, Mrasek K, Kosyakova N (2013) Multicolor FISH methods in current clinical diagnostics. Expert Rev Mol Diagn 13:251-255.
• Liehr T, Othman MA, Rittscher K (2017) Multicolor Karyotyping and Fluorescence In Situ Hybridization-Banding (MCB/mBAND). Methods Mol Biol 1541: 181-187.
• Lim G, Karaskova J, Vukovic B, Bayani J, Beheshti B, Bernardini M, Squire JA, Zielenska M (2004) Combined spectral karyotyping, multicolor banding, and microarray comparative genomic hybridization analysis provides a detailed characterization of complex structural chromosomal rearrangements associated with gene amplification in the osteosarcoma cell line MG-63. Cancer Genet Cytogenet 153:158-164.
• Lim G, Karaskova J, Beheshti B, Vukovic B, Bayani J, Selvarajah S, Watson SK, Lam WL, Zielenska M, Squire JA (2005) An integrated mBAND and submegabase resolution tiling set (SMRT) CGH array analysis of focal amplification, microdeletions, and ladder structures consistent with breakage-fusion-bridge cycle events in osteosarcoma. Genes Chr Cancer 42: 392-403.
• Lin SY, Lee CN, Peng AY, Yuan TJ, Lee DJ, Lin WH, Ma GC, Chen M (2018) Application of molecular cytogenetic techniques to characterize the aberrant Y chromosome arising de novo in a male fetus with mosaic 45,X and solve the discrepancy between karyotyping, chromosome microarray, and multiplex ligation dependent probe amplification. J Formos Med Assoc 117:1027-1031.
• Livingston GK, Escalona M, Foster A, Balajee AS (2018) Persistent in vivo cytogenetic effects of radioiodine therapy: a 21-year follow-up study using multicolor FISH. J Radiat Res 21: 1-8.
• Lizcova L, Zemanova Z, Malinova E, Jarosova M, Mejstrikova E, Smisek P, Pospisilova D, Stary J, Michalova K (2010) A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome. Cancer Genet Cytogenet 201:52-56.
• Macedo Silva ML, Land M, Heller A, Abdelhay E, do Socorro Pombo-de-Oliveira M, Ribeiro R, Alves G, Lerner D, Liehr T (2005) New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcome. Oncol Rep 14: 663-666.
• Macedo Silva ML, Raimondi SC, Abdelhay E, Gross M, Mkrtchyan H, de Figueiredo AF, Ribeiro RC, de Jesus Marques-Salles T, Sobral ES, Gerardin Land MP, Liehr T (2008) Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo. Cancer Genet Cytogenet 182:56-60
• MacKinnon RN, Campbell LJ (2005) A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies. Cancer Genet Cytogenet 163:176-179.
• Mackinnon RN, Campbell LJ (2007) Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20. Cytogenet Genome Res 119:211-220
• MacKinnon RN, Zordan A, Campbell LJ (2005) Recurrent duplication of Xq27-qter in hematological malignancies revealed by multicolor fluorescence in situ hybridization and multicolor banding. Cancer Genet Cytogenet 161:125-129.
• Mackinnon RN, Campbell LJ (2013) Chromothripsis under the microscope: a cytogenetic perspective of two cases of AML with catastrophic chromosome rearrangement. Cancer Genet 206: 238-251.
• MacKinnon RN, Patsouris C, Chudoba I, Campbell LJ (2007) A FISH comparison of variant derivatives of the recurrent dic(17;20) of myelodysplastic syndromes and acute myeloid leukemia: Obligatory retention of genes on 17p and 20q may explain the formation of dicentric chromosomes. Genes Chromosomes Cancer 46:27-36.
• Manolakos E, Sifakis S, Sotiriou S, Peitsidis P, Eleftheriades M, Mersinias V, Liehr T, Thomaidis L, Kitsos G, Papoulidis I, Petersen MB, Orru S. Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature. Clin Dysmorphol 2012, 21:101-105.
• Manolakos M, Vetro A, Papadopoulou E, Kefalas K, Lagou M, Thomaidis L, Peitsidis P, Sifakis S, Divane A, Ziegler M, Liehr T, Zuffardi O, Papoulidis I (2013) Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four break rearrangement. Cytogenet Genome Res 140: 12-20.
• Manvelyan M, Schreyer I, Hols-Herpertz I, Kohler S, Niemann R, Hehr U, Belitz B, Bartels I, Gotz J, Huhle D, Kossakiewicz M, Tittelbach H, Neubauer S, Polityko A, Mazauric ML, Wegner R, Stumm M, Kupferling P, Suss F, Kunze H, Weise A, Liehr T, Mrasek K (2007) Forty-eight new cases with infertility due to balanced chromosomal rearrangements: Detailed molecular cytogenetic analysis of the 90 involved breakpoints. Int J Mol Med 19:855-64.
• Manvelyan M, Hunstig F, Mrasek K, Bhatt S, Pellestor F, Weise A, Liehr T (2008) Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon.Mol Cytogenet. 2008 Apr 29;1:9.
• Manvelyan M, Hunstig F, Bhatt S, Mrasek K, Pellestor F, Weise A, Simonyan I, Aroutiounian R, Liehr T (2008) Chromosome distribution in human sperm - a 3D multicolor banding-study. Mol Cytogent 1:25.
• Manvelyan M, Kempf P, Weise A, Mrasek K, Heller A, Lier A, Höffken K, Fricke HJ, Sayer HG, Liehr T, Mkrtchyan H (2009) Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics. Int J Mol Med 24:335-341.
• Matos RRC, Mkrchyan H, Amaral BA, Liehr T, de Souza MT, Ney-Garcia DR, Santos N, Marques-Salles TJ, Ribeiro RC, Figueiredo AF, Silva MLM (2013) An unusual cytogenetic rearrangement originating from two different abnormalities in chromosome 6 in a child with acute promyelocytic leukemia. Acta Hematologica 130:23-26.
• Matoso E, Melo JB, Ferreira SI, Jardim A, Castelo TM, Weise A, Carreira IM (2013) Insertional translocation leading to a 4q13 duplication including the EPHA5 gene in two siblings with attention-deficit hyperactivity disorder. Am J Med Genet A 161A:1923-1928.
• Melichercikova J, Brezinova J, Zemanova Z, Cermak J, Michalova K (2007) Molecular cytogenetic analysis of complex karyotypes with derivative chromosome der(1)t(1;5) found in two patients with myeloid leukemia. Cancer Genet Cytogenet 176:150-155
• Mkrtchyan H, Glaser M, Gross M, Wedding U, Hoffken K, Liehr T, Karst C, Aroutiounian R (2006) Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2). Cytogenet Genome Res 114:270-273.
• Mkrtchyan H, Garcia Ney DR, de Ventura ES, Liehr T, Felix GR, de Jesus Marques-Salles T, Abdelhay E, Macedo Silva ML (2010) Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia. Cancer Genet Cytogenet 197:71-74.
• Mkrtchyan H, Scheler S, Klein I, Fahr A, Couraud PO, Romero IA, Weksler B, Liehr T (2009) Molecular cytogenetic characterization of the human cerebral microvessel endothelial cell line hCMEC/D3. Cytogenet Genome Res 126:313-317
• Michalova K, Zemanova Z, Brezinova J (2001) [Multicolor fluorescence in situ hybridization (mFISH]. Cas Lek Cesk 140: 99-103. Czech
• Michalova K, Zemanova Z, Brezinova J (2002) Analysis of structural chromosomal aberrations by mFISH and mBAND techniques. In: Early prenatal diagnosis, fetal cells and DNA in the mother - present state and perpectives. The Karolinum Press, Prag, pp 284-292, ISBN: 80-246-0397-7.
• Mitchell CR, Azizova TV, Hande MP, Burak LE, Tsakok JM, Khokhryakov VF, Geard CR, Brenner DJ (2004) Stable intrachromosomal biomarkers of past exposure to densely ionizing radiation in several chromosomes of exposed individuals. Radiat Res 162: 257-263.
• Mkrtchyan H, Glaser M, Gross M, Wedding U, Höffken K, Liehr T, Karst C, Aroutiounian R (2006) Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2). Cytogenet Genome Res 114:270-273.  
• Moghe GA, Kaur MS, Thomas AM, Raseswari T, Swapna M, Rao L (2010) The role of 9qh+ in phenotypic and genotypic heterogeneity in a Van der Woude syndrome pedigree. J Indian Soc Pedod Prev Dent 28:104-109.
• Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Rocchi M, Claussen U, Liehr T (2001) Reconstruction of the female Gorilla gorilla karyotype by Zoo-FISH using 25-color FISH and multicolor banding (MCB). Cytogenet Cell Genet 93: 242-248.
• Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Claussen U, Liehr T (2003) Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding. Int J Mol Med 12:139-146.
• Mrasek K, Krüger G, Bauer I, Müller-Navia J, Liehr T, Weise A (2008) A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences. Cytogenet Genome Res 121:286-287.
• Nazaryan L, Stefanou EG, Hansen C, Kosyakova N, Bak M, Sharkey FH, Mantziou T, Papanastasiou AD, Velissariou V, Liehr T, Syrrou M, Tommerup N (2014) The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2. Europ J Hum Genet 22: 338-343.
• Ney-Garcia DR, Liehr T, Bhatt S, de Souza MT, de Matos RR, Pimenta G, Pulcheri W, Ribeiro RC, Abdelhay E, Silva MLM. Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11. Int J Hematol 2012, 95:112-114.
• Ney-Garcia DR, Liehr T, Bhatt S, de Souza MT, Capela de Matos RR, Binato R, Jordy FC, Abdelhay E, Ribeiro RC, Silva MLM (2012) Molecular cytogenetic studies reveal an unexpected chromosomal inversion as a variant of t(12;21)(p13;q22) in a child with B-cell precursor acute lymphoblastic leukemia. Leuk Lymphoma 53: 342-344.
• Ney-Garcia DR, Vieira TP, Liehr T, Bhatt S, de Souza MT, de Figueiredo AF, Ribeiro RC, Silva MLM (2013) A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone. Blood Cells Mol Dis 50:131-133.
• Ney Garcia DR, Vieira TP, Liehr T, Abdelhay E, Binato R, Neves F, de Souza MT, Ribeiro RC, Silva MLM (2013) Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia. Atlas Genet Cytogenet Oncol Haematol URL : http://AtlasGeneticsOncology.org/Reports/t1919p13q13NeyGarciaID100072.html
• Ney Garcia DR, Liehr T, Emerenciano M, Meyer C, Marschalek R, Pombo-de-Oliveira Mdo S, Ribeiro RC, Poirot Land MG, Macedo Silva ML (2015) Molecular studies reveal MLL-MLLT3 gene fusion displaced in a case of childhood acute lymphoblastic leukemia with complex karyotype. Cancer Genet 208: 143-147.
• Ney Garcia DR, de Souza MT, de Figueiredo AF, Othman MAK, Rittscher K, Abdelhay E, Capela de Matos RR, Meyer C, Marschalek R, Land MGP, Liehr T, Ribeiro RC, Silva MLM (2017) Molecular characterization of KMT2A fusion in 13 cases of pediatric leukemia with a complex or cryptic karyotype. Hem Oncol 35: 760-768.
• Nietzel A, Albrecht B, Starke H, Heller A, Gillessen-Kaesbach G, Claussen U, Liehr T (2003) Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report. J Med Genet 40-E28:1-4.
• Obe G, Durante M (2010) DNA double strand breaks and chromosomal aberrations. Cytogenet Genome Res 128:8-16.
• Othman MAK, Rincic M, Melo JB, Carreira IM, Alhourani E, Hunstig, Glaser A, Liehr T (2014) A novel cryptic three-way translocation t(2;9;18)(p23.2;p21.3;q21.33) with deletion of tumor suppressor genes in 9p21.3 and 13q14 in a T-cell acute lymphoblastic leukemia. Leuk Res Treatment 2014: 357123.
• Othman MAK, Melo JB, Carreira IM, Rincic M, Alhourani E, Wilhelm K, Gruhn B, Glaser A, Liehr T (2015) MLLT10 and IL3 rearrangement together with a complex four-way-translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia. Oncol Rep 33: 625-630.
• Othman MAK, Vujić D, Zecević , Đurišić M, Slavković B, Meyer B, Liehr T (2015) A cryptic three-way translocation t(10;19;11)(p12.31;q13.31;q23.3) with a derivative Y-chromosome in an infant with acute myeloblastic leukemia (M5b). Gene 563: 115-119.
• Othman MAK, Grygalewicz B, Pienkowska-Grela B, Rincic M, Rittscher K, Melo JB, Carreira IM, Meyer B, Marzena W, Liehr T (2015) Novel cryptic rearrangements in adult B cell precursor acute lymphoblastic leukemia involving MLL gene. J Histochem Cytochem 63: 384-390.
• Othman MAK, Melo JB, Carreira IM, Rincic M, Glaser A, Grygalewicz B, Gruhn B, Wilhelm K, Rittscher K, Meyer B, Silva MLM, de Jesus Marques Salles T, Liehr T (2015) High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia. Mol Cytogenet 8: 45.
• Othman MAK, Grygalewicz B, Pienkowska-Grela B, Rygier J, Ejduk A, Rincic M, Melo JB, Carreira IM, Meyer B, Liehr T (2016) A new IGH@ gene rearrangement associated with CDKN2A/B deletion in a young adult B-cell acute lymphoblastic leukemia (B-ALL). Oncol Lett 11: 2117-2122.
• Paderova J, Orlic-Milacic M, Yoshimoto M, da Cunha Santos G, Gallie B, Squire JA (2007) Novel 6p rearrangements and recurrent translocation breakpoints in retinoblastoma cell lines identified by spectral karyotyping and mBAND analyses. Cancer Genet Cytogenet 179:102-111.
• Pandita A, Bayani J, Paderova J, Marrano P, Graham C, Barrett M, Prasad M, Zielenska M, Squire JA (2011) Integrated cytogenetic and high-resolution array CGH analysis of genomic alterations associated with MYCN amplification. Cytogenet Genome Res 134:27-39.
• Park TS, Song J, Lee KA, Min YH, Lee SG, Park Y, Kim J, Lee EY, Choi JR (2008) Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis. Cancer Genet Cytogenet 183:72-76.
• Park TS, Song J, Lee KA, Kim J, Kim SJ, Lee JH, Choi JR, Cheong JW, Park R, Hwang SH, Lee EY (2008) Complex t(8;19;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia. Cancer Genet Cytogenet 185:109-112.
• Park IY, Shin JC, Kwon JY, Koo BK, Kim M, Lim J, Kim Y, Han K (2009) Prenatal diagnosis of Pallister-Killian syndrome associated with pulmonary stenosis and right ventricular dilatation. Korean J Lab Med 29:366-370.
• Papadopoulou E, Sifakis S, Sarri C, Gyftodimou J, Liehr T, Mrasek K, Kalmanti M, Petersen MB (2006) A report of pure 7p duplication syndrome and review of the literature. Am J Med Genet A 140A:2802-2806.
• Pietrzak J, Mrasek K, Obersztyn E, Stankiewicz P, Kosyakova N, Weise A, Cheung S Wai, Cai W Wen, Eggeling F von, Mazurczak T, Bocian E, Liehr T (2007) Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients. J Appl Genet 48:167-175.
• Pignalosa D, Lee R, Hartel C, Sommer S, Nikoghosyan A, Debus J, Ritter S, Durante M (2013) Chromosome inversions in lymphocytes of prostate cancer patients treated with X-rays and carbon ions. Radiother Oncol 109:256-261.
• Polityko A, Maltseva O, Rumyantseva N, Khurs O, Seidel J, Claussen U, Weise A, Liehr T, Starke H (2004) Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3. Int J Mol Med 14:977-979.
• Polityko A, Starke H, Rumyantseva N, Claussen U, Liehr T, Raskin S (2005) Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding. Cytogenet Genome Res 111: 171-174.
• Polityko AD, Khurs OM, Kulpanovich AI, Mosse KA, Solntsava AV, Rumyantseva NV, Naumchik IV, Liehr T, Weise, Mkrtchyan H (2009) Paternally derived der(7)t(Y;7)(p11.1~11.2;p22.3)dn in a mosaic case with Turner syndrome. Europ J Med Gen 52:207-210.
• Popovici C, Basset C, Bertucci F, Orsetti B, Adelaide J, Mozziconacci MJ, Conte N, Murati A, Ginestier C, Charafe-Jauffret E, Ethier SP, Lafage-Pochitaloff M, Theillet C, Birnbaum D, Chaffanet M (2002) Reciprocal translocations in breast tumor cell lines: Cloning of a t(3;20) that targets the FHIT gene. Genes Chromosomes Cancer 35: 204-218.
• Pramparo T, de Gregori M, Gimelli S, Ciccone R, Frondizi D, Liehr T, Pellacani S, Masi G, Brovedani P, Zuffardi O, Guerrini R (2008) A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation. Am J Med Genet A 146A:1754-1760.
• Prasad M, Bernardini M, Tsalenko A, Marrano P, Paderova J, Lee CH, Ben-Dor A, Barrett MT, Squire JA (2008) High definition cytogenetics and oligonucleotide aCGH analyses of cisplatin-resistant ovarian cancer cells. Genes Chromosomes Cancer 47:427-436.
• Rayeroux KC, Campbell LJ (2009) Gene amplification in myeloid leukemias elucidated by fluorescence in situ hybridization. Cancer Genet Cytogenet 193:44-53.
• Reichenbach H, Holland H, Dalitz E, Demandt C, Meiner A, Chudoba I, Lemke J, Claussen U, Froster UG (1999) De novo complete trisomy 5p: clinical report and FISH studies. Am J Med Genet 85: 447-451.
• Rincic M, Rados M, Krsnik Z, Gotovac K, Borovecki F, Liehr T, Brecevic L (2016) Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex. Mol Cytogenet 9:19.
• Riordan D, Vust A, Wickstrom DE, Brown J, Chudley AE, Tomkins D, Chudoba I, Dawson AJ (2002) Identification of a dup(5)(p15.3) by multicolor banding. Clin Genet 61: 277-282.
• Robinson HM, Harrison CJ, Moorman AV, Chudoba I, Strefford JC (2007) Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle. Genes Chromosomes Cancer 46: 318-326.
• Rodriguez L, Starke H, Guardia NM, Tönnies H, Neitzel H, Kozlowski P, Mazauric ML, Heller A, Grondona FL, Mansilla E, Santos Munoz MJ, Liehr T, Martinez-Frias ML (2005) Three new cases with a supernumerary ring chromosome 1. Clin Dysmorphol 14:169-175.
• Rodríguez L, Bhatt SS, García-Castro M, Plasencia A, Fernández-Toral J, Abarca E, de Bello Cioffi M, Liehr T (2014) A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion. Gene 535:165-169.
• Rosenhahn J, Weise A, Michel S, Hennig K, Hartmann I, Schiefner J, Schubert K, Liehr T, von Eggeling F, Loncarevic IF (2007) Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R. Int J Oncol 31:121-128.
• Rudolph C, Steinemann D, Von Neuhoff N, Gadzicki D, Ripperger T, Drexler HG, Mrasek K, Liehr T, Claussen U, Emura M, Schröck E, Schlegelberger B (2004) Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519. Cancer Genet Cytogenet 153: 144-150.
• Rudolph C, Liehr T, Steinemann D, Emura M, Daibata M, Matsuo Y, Emi N, Abe M, Lai R, Mrasek K, Claussen U, Schlegelberger B (2006) Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanisms. Cytogenet Genome Res 112: 213-221.
• Sangpakdee W, Tanomtong A, Fan X, Pinthong K, Weise A, Liehr T (2016) Application of multicolor banding combined with heterochromatic and locus-specific probes identify evolutionary conserved breakpoints in Hylobates pileatus. Mol Cytogenet 9: 17.
• Sangpakdee W, Tanomtong A, Chaveerach A, Pinthong K, Trifonov V, Loth K, Hensel C, Liehr T, Weise A, Fan X (2018) Molecular cytogenetic analysis of one African and five Asian macaque species reveals identical karyotypes as in mandrill. Curr Genomics 19:207-215.
  
• Sarri C, Gyftodimou Y, Grigoriadou M, Pandelia E, Kalogirou S, Kokotas H, Mrasek K, Weise A, Petersen MB (2006) Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face. Cytogenet Genome Res 114:330-337.
• Sárová I, Brezinová J, Zemanová Z, Lizcová L, Berková A, Izáková S, Malinová E, Fuchs O, Kostecka A, Provazníková D, Filkuková J, Maaloufová J, Starý J, Michalová K (2009) A partial nontandem duplication of the MLL gene in four patients with acute myeloid leukemia. Cancer Genet Cytogenet 195:150-156.
• Sárová I, Brezinová J, Zemanová Z, Izáková S, Lizcová L, Malinová E, Berková A, Cermák J, Maaloufová J, Nováková L, Michalová K (2010) Cytogenetic manifestation of chromosome 11 duplication/amplification in acute myeloid leukemia. Cancer Genet Cytogenet 199:121-127.
• Sarova I, Brezinova J, Zemanova Z, Bystricka D, Krejcik Z, Soukup P, Vydra J, Cermak J, Jonasova A, Michalova K (2013) Characterization of chromosome 11 breakpoints and the areas of deletion and amplification in patients with newly diagnosed acute myeloid leukemia. Genes Chromosomes Cancer 52:619-635.
• Sarova I, Brezinova J, Zemanova Z, Ransdorfova S, Izakova S, Svobodova K, Pavlistova L, Berkova A, Cermak J, Jonasova A, Siskova M, Michalova K (2016) Molecular cytogenetic analysis of dicentric chromosomes in acute myeloid leukemia. Leuk Res 43: 51-57.
• Sauter S, Von Beust G, Burfeind P, Weise A, Starke H, Liehr T, Zoll B (2003) Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10]. Am J Med Genet 120A: 533-536.
• Schaeferhenrich A, Beyer-Sehlmeyer G, Festag G, Kuechler A, Haag N, Weise A, Liehr T, Claussen U, Marian B, Sendt W, Scheele J, Pool-Zobel BL (2003) Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal. Mutat Res 526: 19-32.
• Schmidt S, Claussen U, Liehr T, Weise A (2005) Evolution versus constitution: differences in chromosomal inversion. Hum Genet 117: 213-219.
• Schmidt T, Bartels I, Liehr T, Burfeind P, Zoll B, Shoukiera M (2013) A family with an inverted tandem duplication 5q22.1-q23.2. Cytogenet Genome Res 139:65-70.
• Schmidt T, Bierhals T, Kortüm F, Bartels I, Liehr T, Burfeind P, Shoukier M, Frank V, Bergmann C, Kutsche K (2014) Branchio-Otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8. Cytogenet Genome Res 142:1-6.
• Schmitz S, Pinkawa M, Eble MJ, Kriehuber R (2013) Persisting ring chromosomes detected by mFISH in lymphocytes of a cancer patient-a case report. Mutat Res 756:158-164.
• Schreyer I, Neumann A, Beensen V, Eichhorn KH, Heller A, Claussen U, Liehr T (2005) Dup(13)(q14.2-q14.3): yet another new differential diagnostic aspect for short stature-like phenotype. J Histochem Cytochem 53:365-366.
• Schulten HJ, Perske C, Thelen P, Polten A, Borst C, Gunawan B, Nagel H (2007) Establishment and characterization of two distinct malignant mesothelioma cell lines with common clonal origin. Cancer Genet Cytogenet 176:35-47.
• Seidel J, Heller A, Senger G, Starke H, Chudoba I, Kelbova C, Tönnies H, Neitzel H, Haase C, Beensen V, Zintl F, Claussen U, Liehr T (2003) A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behavior disorder characterized comprehensively by molecular cytogenetics-Case report and review of the literature Europ. J. Pedriat  162: 582-588.
• Selvarajah S, Yoshimoto M, Maire G, Paderova J, Bayani J, Squire JA, Zielenska M (2007) Identification of cryptic microaberrations in osteosarcoma by high-definition oligonucleotide array comparative genomic hybridization. Cancer Genet Cytogenet 179:52-61
• Seller MJ, Bint S, Kavalier F, Brown RN, Ogilvie CM (2006) Multicolor banding detects a complex three chromosome, seven breakpoint unbalanced rearrangement in an ICSI-derived fetus with multiple abnormalities. Am J Med Genet A 140A:1102-1107.
• Serra A, Schackert HK, Mohr B, Weise A, Liehr T, Fitze G (2007) t(11;19)(q21;p12~p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinoma. J Pediatr Surg 42:E23-29.
• Sifakis S, Eleftheriades M, Kappou D, Murru R, Konstantinidou A, Orru S, Ziegler M, Liehr T, Manolakos E, Papoulidis I (2014) Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature. Birth Defects Res A Clin Mol Teratol 100:284-293.
• Sotnik NV, Azizova TV, Osovets SV (2011) [Structural genomic damages in workers of plutonium production]. Radiats Biol Radioecol 51:213-217. Russian.
• Soysal Y, Balci S, Hekimler K, Liehr T, Ewers E, Schoumans J, Bui TH, Içduygu FM, Kosyakova N, Imirzalioğlu N (2009) Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy. Am J Med Genet A 149A:2782-2787.
• Stankiewicz P, Kuechler A, Eller CD, Sahoo T, Baldermann C, Lieser U, Hesse M, Glaser C, Hagemann M, Yatsenko SA, Liehr T, Horsthemke B, Claussen U, Marahrens Y, Lupski JR, Hansmann I (2006) Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation. Am J Med Genet A 140:442-452.
• Starke H, Raida M, Trifonov V, Clement JH, Loncarevic IF, Heller A, Bleck C, Nietzel A, Rubtsov N, Claussen U, Liehr T (2001) Molecular cytogenetic characterization of an acquired supernumerary minute marker chromosome as sole abnormality in a case clinically diagnosed as Philadelphia negative chronic myelogenous leukaemia. Br J Haematol 113: 435-438.
• Starke H, Senger G, Kossakiewicz M, Tittelbach H, Rau D, Rubtsov N, Trifonov V, Heller A, Hartmann I, Claussen U, Liehr T. Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB). Prenat Diag 21: 1049-1052.
• Starke H, Mitulla B, Beensen V, Trifonov V, Rubtsov N, Heller A, Ziegler M, Neumann A, Claussen U, Liehr T (2003) First postnatal case of mosaic del(22)/r(22). Prenat Diagn 23:765-7.
• Starke H, Nietzel A, Weise A, Heller A, Mrasek K, Belitz B, Kelbova C, Volleth M, Albrecht B, Mitulla B, Trappe R, Bartels I, Adolph S, Dufke A, Singer S, Stumm M, Wegner RD, Seidel J, Schmidt A, Kuechler A, Schreyer I, Claussen U, von Eggeling F, Liehr T (2003) Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification. Hum Genet 114:51-67.
• Struski S, Helias C, Gervais C, Audhuy B, Zamfir A, Herbrecht R, Lessard M (2007) 13q deletions in B-cell lymphoproliferative disorders: frequent association with translocation. Cancer Genet Cytogenet 174:151-160.
• Stumm M, Musebeck J, Tonnies H, Volleth M, Lemke J, Chudoba I, Wieacker P (2002) Partial trisomy 9p12p21.3 with a normal phenotype. J Med Genet 39: 141-144.
• Thienpont B, Gewillig M, Fryns JP, Devriendt K, Vermeesch J (2006) Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies. Cytogenet Genome Res 114:338-341.
• Tjia WM, Hu L, Zhang MY, Guan XY (2007) Characterization of rearrangements involving 4q, 13q and 16q in hepatocellular carcinoma cell lines using region-specific multiplex-FISH probes. Cancer Lett 250:92-99
• Tönnies H, Stumm M, Wegner R-D, Chudoba I, Kalscheur V, Neitzel H (2001) Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostic. Cytogenet Cell Genet 93: 188-194.
• Tönnies H (2005) Molecular cytogenetics in molecular diagnostics. In Molecular Diagnostics, Ed. Patrinos and Ansorge: 139-157.
• Tönnies H, Gerlach A, Heineking B, Starke H, Neitzel H, Neumann LM (2006) Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13. Cytogenet Genome Res 114:325-329.
• Trappe R, Bohm D, Kohlhase J, Weise A, Liehr T, Essers G, Meins M, Zoll B, Bartels I, Burfeind P (2002) A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis. Cytogenet Genome Res 98: 1-8.
• Trifonov V, Seidel J, Starke H, Martina P, Beensen V, Ziegler M, Hartmann I, Heller A, Nietzel A, Claussen U, Liehr T (2003) Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter. Prenat Diagn 23: 427-430.
• Trimborn M, Liehr T, Belitz B, Pfeiffer L, Varon R, Neitzel H, Tönnies H (2005) Prenatal diagnosis and molecular cytogenetic characterization of an unusual complex structural rearrangement in a pregnancy following intracytoplasmic sperm injection (ICSI). J Histochem Cytochem 53:351-354
• Tsarouha H, Kyriazoglou AI, Ribeiro FR, Teixeira MR, Agnantis N, Pandis N (2006) Chromosome analysis and molecular cytogenetic investigations of an epithelioid hemangioendothelioma. Cancer Genet Cytogenet 169:164-168.
• Tzschach A, Ramel C, Kron A, Seipel B, Wüster C, Cordes U, Liehr T, Hoeltzenbein M, Menzel C, Ropers HH, Ullmann R, Kalscheuer V, Decker J, Steinberger D (2009) Hypergonadotropic hypogonadism in a patient with inv ins (2;4). Int J Androl 32:226-230.
• Utine GE, Aktas D, Alanay Y, Gücer S, Tuncbilek E, Mrasek K, Liehr T (2007) Distal partial trisomy 1q: report of two cases and a review of the literature. Prenat Diagn 27:865-871.
• Vičić A, Zudenigo D, Korać P, Liehr T, Stipoljev F (2013) Prenatally detected interstitial deletion 13q12.3-q22 in a fetus with a cystic hygroma. Gene 531: 90-91.
• Vlckova M, Trkova M, Zemanova Z, Hancarova M, Novotna D, Raskova D, Puchmajerova A, Drabova J, Zmitkova Z, Tan Y, Sedlacek Z (2012) Mechanism and genotype-phenotype correlation of two proximal 6q deletions characterized using mBAND, FISH, array CGH, and DNA sequencing. Cytogenet Genome Res 136:15-20.
• Volleth M, Stumm M, Kalscheuer VM, Reschke K, Liehr T, Wieacker P (2003) Premature ovarian failure in a woman with an unusual pseudoisodicenric X chromosome. Ger J Obstet Gynecol 63:1054-1057
• Vorsanova SG, Iourov IV, Voinova-Ulas VV, Weise A, Monakhov VV, Kolotii AD, Soloviev IV, Novikov PV, Liehr T, Yurov YB (2008) Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature. Mol Cytogenet 1(1):13.
• Vorsanova SG, Yurov YB, Iourov IY (2010) Human interphase chromosomes: a review of available molecular cytogenetic technologies. Mol Cytogenet 11;3:1.
• Vukovic B, Beheshti B, Park P, Lim G, Bayani J, Zielenska M, Squire JA (2007) Correlating breakage-fusion-bridge events with the overall chromosomal instability and in vitro karyotype evolution in prostate cancer. Cytogenet Genome Res 116:1-11.
• Wafa A, Aljapawe A, Othman MAK, Liehr T, Alhourani E, Al Achkar W (2014) Do novo del(9)(p13) in a childhood T-cell prolymphocytic leukemia as sole abnormality. Exp Hematol Oncol 3: 28.
• Wafa A, Asa'ad M, Ikhtiar A, Liehr T, Al-Achkar W (2015) Deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: a rare event. Mol Cytogenet 8:59.
• Wafa A, Moassass F, Liehr T, Bhatt S, Aljapawe A, Al Achkar W (2016) A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia. Mol Cytogenet 9: 91.
• Wafa A, Moassass F, Liehr T, Aljapawe A, Al Achkar W (2016) Partial trisomy 1q21-qter and partial monosomy 7q21-qter due to a derivative chromosome 7 in myelodysplastic syndrome associated with squamous cell carcinoma: Case report. Case Rep Clin Med 5: 518-527.
• Wafa A, Moassass F, Liehr T, Al-Ablog A, Al-Achkar W (2016) Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report. J Med Case Rep 10: 203.
• Wafa A, Assad M, Liehr T, Aljapawe A, Al Achkar W (2016) A new complex karyotype in a unique de novo myelodysplastic syndrome case involving ten chromosomes and monoallelic loss of TP53. Gene Rep 4: 208-212.
• Wafa A, As’sad M, Liehr T, Aljapawe A, Al-Achkar W (2017) Childhood pre-B-acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6 and 13. J Med Case Rep 11: 94.
• Wafa A, Almedani S, Liehr T, Ziegler M, Aljapawe A, Al Achkar W (2017) Complex karyotype involving six chromosomes, with one dicentric and three yet unreported acquired chromosomal aberrations in a case of splenic marginal zone lymphoma. Gene Rep 8: 79-83.
• Wafa A, ALmedania S, Aljapawe A, Liehr T, Soulaiman SE, Mouna R, Othman MAK, ALachkar W (2018) A new adult AML case with an extremely complex karyotype, remission and relapse combined with high hyperdiploidy of a normal chromosome set in secondary AML. BMC Hematol 18:21.
• Weise A, Starke H, Heller A, Claussen U, Liehr T (2002) Evidence for interphase DNA decondensation transverse to the chromosome axis: A multicolor banding analysis. Int J Mol Med, 9: 359-361.
• Weise A, Starke H, Heller A, Tönnies H, Volleth M, Stumm M, Senger G, Nietzel A, Claussen U, Liehr T (2002) Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes. J Med Genet 39: 434-439.
• Weise A, Heller A, Starke H, Mrasek K, Kuechler A, Pool-Zobel BL, Claussen U, Liehr T (2003) Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method. Cytogenet Genome Res 103:34-9.
• Weise A, Starke H, Mrasek K, Claussen U, Liehr T (2005) New insights into the evolution of chromosome 1. Cytogenet Genome Res 108: 217-222.
• Weise A, Mrasek K, Fickelscher I, Claussen U, Cheung SW, Cai WW, Liehr T, Kosyakova N (2008) Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set. J Histochem Cytochem 56:487-493.
• Yurov YB, Iourov IY, Vorsanova SG, Liehr T, Kolotii AD, Kutsev SI, Pellestor F, Beresheva AK, Demidova IA, Kravets VS, Monakhov VV, Soloviev IV (2007) Aneuploidy and confined chromosomal mosaicism in the developing human brain. PLoS ONE 2:e558.
• Yurov YB, Iourov IY, Vorsanova SG, Demidova IA, Kravetz VS, Beresheva AK, Kolotii AD, Monakchov VV, Uranova NA, Vostrikov VM, Soloviev IV, Liehr T (2008) The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1. Schizophr Res 98:139-147.
• Yurov YB, Vorsanova SG, Iourov IY (2013) Human Interphase Chromosomes - Biomedical Aspects. Springer.
• Yurov YB, Vorsanova SG, Liehr T, Kolotii AD and Iourov IY (2014) X chromosome aneuploidy in the Alzheimer's disease brain. Mol Cytogenet 7: 20.
• Yurov YB, Vorsanova SG, Demidova IA, Kolotii AD, Soloviev IV, Iourov IY. Mosaic brain aneuploidy in mental illnesses: An association of low-level post-zygotic aneuploidy with schizophrenia and comorbid psychiatric disorders. Curr Genomics. 2018 Apr;19(3):163-172.
• Zahnreich S, Krunic D, Melnikova L, Szejka A, Drossel B, Sabatier L, Durante M, Ritter S, Fournier C (2012) Duplicated chromosomal fragments stabilize shortened telomeres in normal human IMR-90 cells before transition to senescence. J Cell Physiol 227: 1932-1940.
• Zahnreich S, Krunic D, Melnikova L, Szejka A, Drossel B, Sabatier L, Durante M, Ritter S, Fournier C (2012) Duplicated chromosomal fragments stabilize shortened telomeres in normal human IMR-90 cells before transition to senescence. J Cell Physiol 227:1932-1940.
• Zivkovic T, Chudoba I, Bokemeyer C, Dierlamm J (2006) Multicolour banding provides a detailed characterisation of structural abnormalities of chromosome 1 in Burkitt lymphoma. Br J Haematol 132:2.
• Zuna J, Zaliova M, Muzikova K, Meyer C, Lizcova L, Zemanova Z, Brezinova J, Votava F, Marschalek R, Stary J, Trka J (2010) Acute leukemias with ETV6/ABL1 (TEL/ABL) fusion: poor prognosis and prenatal origin. Genes Chromosomes Cancer 49:873-884.