Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorder

Early Human Development

Volumn 83, Issue 7, 2007, Pages 471-478

  Dudley, Oenone ^a   Muscatelli, F ^a  

^a CNRS   (France)

Author keywords

Imprinting; Intrauterine; ; Phenotype; ; Prader Willi syndrome;

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CESAREAN SECTION; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; FEMALE; FETUS DEVELOPMENT; FETUS GROWTH; FRANCE; GENE DELETION; GENOME IMPRINTING; GROWTH RETARDATION; HUMAN; HYDRAMNIOS; INTELLECTUAL IMPAIRMENT; LABOR INDUCTION; LOW BIRTH WEIGHT; MAJOR CLINICAL STUDY; MALE; MATERNAL AGE; MUSCLE HYPOTONIA; OBESITY; PRADER WILLI SYNDROME; SMALL FOR DATE INFANT; SPONTANEOUS ABORTION; UNIPARENTAL DISOMY;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; DNA; FEMALE; FETAL GROWTH RETARDATION; GENOMIC IMPRINTING; HUMANS; INFANT; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; MALE; MIDDLE AGED; PRADER-WILLI SYNDROME; PREGNANCY; PREGNANCY COMPLICATIONS;

EID: 34249328483     PISSN: 03783782     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.earlhumdev.2006.09.002     Document Type: Article

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