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ChromosOmics - Database
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CHROMOSOME 12 -
-
paternal UPD -
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|
pat UPD-cases
without clinical findings + normal karyotype
|
case no.
|
gender
|
age at diagnosis
|
studied
material
|
GTG-banding result
|
clinical symptoms
|
reference
|
12-
OpU-N/
1-1
|
- |
- |
- |
- |
- |
- |
mosaic cases
case no.
|
gender
|
age at
diagnosis
|
studied
material
|
GTG-banding
result
|
clinical
symptoms
|
reference
|
12-
OpU-N/
mos/
1-1
|
- |
- |
- |
- |
- |
- |
|
pat UPD-cases without clinical
findings + balanced karyotype |
case no.
|
gender
|
age at diagnosis
|
studied
material
|
GTG-banding result
|
clinical symptoms
|
reference
|
12-
OpU-bal/
1-1
|
- |
- |
- |
- |
- |
- |
|
pat UPD-cases without clinical
findings + sSMC
|
case no.
|
case no. in
sSMC database
|
gender/
age at diagnosis
|
studied
material
|
GTG-banding
result
|
final FISH
result of the sSMC
|
FISH
methods
|
clinical
symptoms
|
reference
|
12-
OpU-sSMC/
1-1
|
-
|
-
|
-
|
-
|
-
|
-
|
-
|
-
|
|
segmental
pat UPD-cases without clinical findings
|
case no.
|
gender
|
age at diagnosis
|
studied
material
|
GTG-banding result
|
clinical symptoms
|
reference
|
12-
OpU-seg/
/
1-1
|
-
|
-
|
-
|
- |
-
|
- |
mosaic cases
case no.
|
gender
|
age at
diagnosis
|
studied
material
|
GTG-banding
result
|
clinical
symptoms
|
reference
|
12-
OpU-seg/
/
mos/
1-1
|
-
|
-
|
-
|
- |
-
|
- |
|
pat UPD-cases without clinical findings + other
imbalances |
case no.
|
gender
|
age at diagnosis
|
studied
material
|
GTG-banding result
|
clinical symptoms
|
reference
|
12-
OpU-imb/
1-1
|
- |
- |
- |
- |
- |
- |
mosaic cases
case no.
|
gender
|
age at
diagnosis
|
studied
material
|
GTG-banding
result
|
clinical
symptoms
|
reference
|
12-
OpU-imb/
mos/
1-1
|
- |
- |
- |
- |
- |
- |
|
pat
UPD-cases with or unclear clinical correlation +
normal karyotype |
case no.
|
gender
|
age at diagnosis
|
studied
material
|
GTG-banding result
|
clinical symptoms
|
reference
|
12-
WpU-N/
1-1
|
female |
newborn |
PBL |
n.a. |
sulfite
oxidase deficiency (gene SUOX
in 12q13.2) |
{756} |
12-
WpU-N/
2-1
|
female |
5y |
PBL |
46,XX |
DYS and sideroblast anemia
(genes PUS1
and PFKM
in 12q24.32 and 12q13.11) |
{882;
1090; 1219} |
12-
WpU-N/
3-1
|
n.a. |
postnatal |
PBL |
n.a. |
Phenylketonuria
(gene PAH
in 12q23.2) |
{1109} |
12-
WpU-N/
4-1
|
male |
8y
|
PBL |
n.a. |
External ophthalmoplegia
with rib and vertebral anomalies
(gene
MYF5
in
12q21.31) |
{1379} |
mosaic cases
case no.
|
gender
|
age at
diagnosis
|
studied
material
|
GTG-banding
result
|
clinical
symptoms
|
reference
|
12-
WpU-N/
mos/
1-1
|
- |
- |
- |
- |
- |
- |
|
pat
UPD-cases with or unclear clinical correlation+
balanced karyotype
|
case no.
|
gender
|
age at diagnosis
|
studied
material
|
GTG-banding result
|
clinical symptoms
|
reference
|
12-
WpU-bal/
1-1 |
-
|
-
|
-
|
-
|
-
|
-
|
|
pat
UPD-cases with or unclear clinical findings + sSMC
|
case no.
|
case no. in
sSMC database
|
gender/
age at diagnosis
|
studied
material
|
GTG-banding
result
|
final FISH
result of the sSMC
|
FISH
methods
|
clinical
symptoms
|
reference
|
12-
WpU-sSMC/
1-1
|
- |
- |
- |
- |
- |
- |
- |
- |
|
segmental
pat UPD-cases with or unclear clinical correlation
|
case no.
|
gender
|
age at diagnosis
|
studied
material
|
GTG-banding result
|
clinical symptoms
|
reference
|
12-
WpU-seg/
/
1-1
|
- |
- |
- |
- |
- |
- |
mosaic cases
case no.
|
gender
|
age at
diagnosis
|
studied
material
|
GTG-banding
result
|
clinical
symptoms
|
reference
|
12-
WpU-seg/
/
mos/
1-1
|
- |
- |
- |
- |
- |
- |
|
pat UPD-cases with or unclear clinical correlation +
other imbalances |
case no.
|
gender
|
age at diagnosis
|
studied
material
|
GTG-banding result
|
clinical symptoms
|
reference
|
12-
WpU-imb/
1-1
|
- |
- |
- |
- |
- |
- |
mosaic cases
case no.
|
gender
|
age at
diagnosis
|
studied
material
|
GTG-banding
result
|
clinical
symptoms
|
reference
|
12-
WpU-imb/
mos/
1-1
|
- |
- |
- |
- |
- |
- |
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