ChromosOmics - Database

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                   - HM- REFERENCES from Ref. {1} -                                        

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  39. Barber JC, Maloney V, Hollox EJ, Stuke-Sontheimer A, du Bois G, Daumiller E, Klein-Vogler U, Dufke A, Armour JA, Liehr T. Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Eur J Hum Genet 2005; 13:1131–1136.
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  42. Barber JC, Maloney VK, Kirchhoff M, Thomas NS, Boyle TA, Castle B. Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences. Am J Med Genet A 2007; 143:615–618.
  43. Barber JC, Brasch-Andersen C, Maloney VK, Huang S, Bateman MS, Graakjaer J, Heinl UD, Fagerberg C. A novel pseudo-dicentric variant of 16p11.2-q11.2 contains euchromatin from 16p11.2-p11.1 and resembles pathogenic duplications of proximal 16q. Cytogenet Genome Res 2013; 139:59–64.
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