Prader-Willi syndrome: Is there a recognizable fetal phenotype?

Prenatal Diagnosis

Volumn 28, Issue 9, 2008, Pages 796-799

  Bigi, Nicole ^a   Faure, Jean Michel ^b   Coubes, Christine ^a   Puechberty, Jacques ^a   Lefort, Geneviève ^a   Sarda, Pierre ^a   Blanchet, Patricia ^a  

^a MONTPELLIER UNIVERSITY HOSPITAL   (France)

^b HÔPITAL ARNAUD DE VILLENEUVE   (France)

Author keywords

Fetal phenotype; Prader Willi syndrome; Prenatal diagnosis

Indexed keywords

ADULT; ARTICLE; BODY POSITION; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME DELETION; FACE DYSMORPHIA; FEMALE; FETUS; FETUS MOVEMENT; GESTATION PERIOD; HUMAN; HUMAN TISSUE; HYDRAMNIOS; KARYOTYPING; METHYLATION; PHENOTYPE; PRADER WILLI SYNDROME; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; UNIPARENTAL DISOMY;

ADULT; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; POLYHYDRAMNIOS; PRADER-WILLI SYNDROME; PREGNANCY;

EID: 55449100745     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1973     Document Type: Article

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