Pervasive developmental disorders in Prader-Willi syndrome: The Leuven experience in 59 subjects and controls

American Journal of Medical Genetics, Part A

Volumn 140, Issue 11, 2006, Pages 1136-1142

  Descheemaeker, Mie Jef ^a,c   Govers, Veerle ^a   Vermeulen, Peter ^b   Fryns, Jean Pierre ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b Autisme Centraal   (Belgium)

^c Center for Human Genetics   (Belgium)

Author keywords

Autism; Behavioral phenotype; Chromosome 15; Learning disabilities; Mental retardation; Pervasive developmental disorders (PDD); Prader Willi syndrome (PWS); Uniparental maternal disomy (UPD)

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME 15; COMORBIDITY; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; EXPERIENCE; FEMALE; GENOME IMPRINTING; HUMAN; INTELLIGENCE QUOTIENT; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; PERVASIVE DEVELOPMENTAL DISODER MENTALLY RETARDATION SCALE; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; RATING SCALE; SCREENING; SYMPTOMATOLOGY; UNIPARENTAL DISOMY;

ADOLESCENT; ADULT; BELGIUM; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; COMORBIDITY; FEMALE; HUMANS; INTELLIGENCE; INTELLIGENCE TESTS; MALE; MIDDLE AGED; PRADER-WILLI SYNDROME; UNIPARENTAL DISOMY;

EID: 33744805839     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31235     Document Type: Article

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