Prader-Willi syndrome: A study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders

European Child and Adolescent Psychiatry

Volumn 13, Issue 1, 2004, Pages 42-50

  Veltman, Marijcke W M ^a,b   Thompson, Russell J ^a   Roberts, Sian E ^c   Thomas, N Simon ^c   Whittington, Joyce ^a   Bolton, Patrick F ^a,b  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

^c WESSEX REGIONAL GENETICS LABORATORY   (United Kingdom)

Author keywords

ASQ; Autism; Autism spectrum disorders; Prader Willi syndrome

Indexed keywords

ADAPTIVE BEHAVIOR; ADOLESCENT; ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME 15Q; CHROMOSOME DELETION; COGNITION; CONTROLLED STUDY; DAILY LIFE ACTIVITY; DEPTH PERCEPTION; DISEASE ASSOCIATION; FEMALE; GENE EXPRESSION; GENETIC SUSCEPTIBILITY; HEALTH SURVEY; HUMAN; HYPOTHESIS; INFORMATION PROCESSING; MAJOR CLINICAL STUDY; MALE; MOTOR CONTROL; PATHOGENESIS; PRADER WILLI SYNDROME; PREDICTION; QUESTIONNAIRE; SCREENING TEST; SOCIAL ADAPTATION; SYMPTOM; TELEPHONE; UNIPARENTAL DISOMY;

ADOLESCENT; ANALYSIS OF VARIANCE; AUTISTIC DISORDER; CHILD; CHILD BEHAVIOR DISORDERS; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; GENE DELETION; GREAT BRITAIN; HUMANS; INFANT; MALE; POLYMERASE CHAIN REACTION; PRADER-WILLI SYNDROME; PSYCHIATRIC STATUS RATING SCALES; RISK FACTORS; UNIPARENTAL DISOMY;

EID: 1442300775     PISSN: 10188827     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00787-004-0354-6     Document Type: Article

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