Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15

Prenatal Diagnosis

Volumn 23, Issue 11, 2003, Pages 938-943

  L'Hermine, A Coulomb ^a   Aboura, A ^a   Brisset, S ^a   Cuisset, L ^b   Castaigne, V ^a   Labrune, P ^a   Frydman, R ^a   Tachdjian, G ^a  

^a HÔPITAL ANTOINE BÉCLÈRE   (France)

^b Hôpital Cochin ^*  (France)

Author keywords

Chromosome 15; Corpus callosum; Disomy; Genitalia; Prader Willi; Prenatal diagnosis

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; AUTOPSY; CASE REPORT; CHORION VILLUS SAMPLING; CHROMOSOME 15; CORPUS CALLOSUM; EUTROPHICATION; FACE DYSMORPHIA; FEMALE; FETUS; FIRST TRIMESTER PREGNANCY; FOOT; GENITAL SYSTEM; GESTATIONAL AGE; HUMAN; HYPOPLASIA; INTRAUTERINE GROWTH RETARDATION; KARYOTYPE; LATERAL BRAIN VENTRICLE; MALE; MATERNAL AGE; METHYLATION; PHENOTYPE; PRADER WILLI SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SEX CHROMOSOME MOSAICISM; SKELETON MALFORMATION; TRISOMY; TRISOMY 15; ULTRASOUND; UNIPARENTAL DISOMY;

ABORTION, EUGENIC; AMNIOCENTESIS; CHORIONIC VILLI SAMPLING; CHROMOSOMES, HUMAN, PAIR 15; EMBRYONIC AND FETAL DEVELOPMENT; FEMALE; HUMANS; MALE; MATERNAL AGE; MIDDLE AGED; PRADER-WILLI SYNDROME; PREGNANCY; PREGNANCY TRIMESTER, FIRST; PREGNANCY, HIGH-RISK; PRENATAL DIAGNOSIS; UNIPARENTAL DISOMY;

EID: 0344442913     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.732     Document Type: Article

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