Variations in fetal phenotype in Prader-Willi syndrome

Prenatal Diagnosis

Volumn 29, Issue 3, 2009, Pages 294-

  Haugen, Guttorm ^a   Rønnestad, Arild ^a   Kroken, Mette ^b  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b ULLEVÅL UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; CASE REPORT; CLINICAL FEATURE; DOPPLER FLOWMETRY; FETUS; FETUS ECHOGRAPHY; FETUS MOVEMENT; HUMAN; HYDRAMNIOS; INTRAUTERINE GROWTH RETARDATION; LETTER; MALE; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; UNIPARENTAL DISOMY;

EID: 61449140156     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2207     Document Type: Letter

References (2)

1. Bigi N, Faure J-M, Coubes C, et al. 2008. Prader-Willi syndrome: is there a recognizable fetal phenotype? Prenat Diagn 28: 796-799.
2. Dudley O, Muscatelli F. 2007. Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorder. Early Hum Dev 83: 471-478.