TY  - GEN
AU  - Kraoua,Lilia
AU  - Chaabouni,Myriam
AU  - Ewers,Elisabeth
AU  - Chelly,Imen
AU  - Ouertani,Ines
AU  - Ben Jemaa,Lamia
AU  - Maazoul,Faouzi
AU  - Liehr,Thomas
AU  - Chaabouni,Habiba
TI  - Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case report
SN  - 1878-0849
PY  - 2011///1031
KW  - Adolescent
KW  - Angelman Syndrome
KW  - genetics
KW  - Chromosome Banding
KW  - Chromosome Disorders
KW  - Chromosomes, Human, Pair 15
KW  - Humans
KW  - Male
KW  - Membrane Transport Proteins
KW  - Phenotype
KW  - Pigmentation Disorders
KW  - Prader-Willi Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.ejmg.2011.04.007
ER  -