The Beckwith-Wiedemann syndrome phenotype and the risk of cancer

Medical and Pediatric Oncology

Volumn 28, Issue 6, 1997, Pages 411-415

  Schneid, H ^a   Vazquez, M P ^a   Vacher, C ^a   Gourmelen, M ^a   Cabrol, S ^a   Le Bouc, Y ^a  

^a ARMAND TROUSSEAU HOSPITAL   (France)

Author keywords

Beckwith Wiedemann syndrome; insulin like growth factor; tumor

Indexed keywords

SOMATOMEDIN C;

ARTICLE; BECKWITH WIEDEMANN SYNDROME; CANCER INCIDENCE; CANCER RISK; CARCINOGENESIS; CHILD; CHROMOSOME 11P; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE COURSE; FAMILY HISTORY; GENE LOCUS; HEPATOMEGALY; HUMAN; MACROGLOSSIA; NEPHROBLASTOMA; OMPHALOCELE; PHENOTYPE; PRIORITY JOURNAL; RISK ASSESSMENT; SPLENOMEGALY;

BECKWITH-WIEDEMANN SYNDROME; CHILD, PRESCHOOL; FEMALE; HUMANS; INFANT; INSULIN-LIKE GROWTH FACTOR I; INSULIN-LIKE GROWTH FACTOR II; MALE; NEOPLASMS; ODDS RATIO; PHENOTYPE; RISK;

EID: 0030929370     PISSN: 00981532     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-911X(199706)28:6<411::AID-MPO3>3.0.CO;2-J     Document Type: Article

References (23)