Third case of WAGR syndrome with severe obesity and constitutional deletion of chromosome (11)(p12p14) [2]

American Journal of Medical Genetics

Volumn 107, Issue 1, 2002, Pages 70-71

  Gul D ^a   Ogur G ^a   Tunca, Y ^a   Ozcan O ^a  

^a GULHANE SCHOOL OF MEDICINE   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ANIRIDIA; CASE REPORT; CHROMOSOME DELETION; CHROMOSOME DELETION 11; CLINICAL FEATURE; CONGENITAL CATARACT; CYTOGENETICS; DISEASE COURSE; HUMAN; KARYOTYPE; LETTER; MALE; MENTAL DEFICIENCY; NEPHROBLASTOMA; OBESITY; PRIORITY JOURNAL; UROGENITAL TRACT MALFORMATION; WAGR SYNDROME;

ADOLESCENT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 11; HUMANS; MALE; MENTAL RETARDATION; OBESITY; WAGR SYNDROME; WILMS TUMOR;

EID: 0036134782     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10013     Document Type: Letter

References (6)

1. Mutation in the PAX 6 gene in twenty patients with aniridia
2. The molecular genetics of Wilms' tumor
3. Molecular genetics of Wilms' tumor
4. Obesity: A new feature of WAGR (del 11p) syndrome
5. Obesity and WAGR syndrome