Autism spectrum disorders and hyperactive/impulsive behaviors in Japanese patients with Prader-Willi syndrome: A comparison between maternal uniparental disomy and deletion cases

American Journal of Medical Genetics, Part A

Volumn 164, Issue 9, 2014, Pages 2180-2186

  Ogata, Hiroyuki ^a   Ihara, Hiroshi ^a   Murakami, Nobuyuki ^a   Gito, Masao ^a,b   Kido, Yasuhiro ^a   Nagai, Toshiro ^a  

^a DOKKYO MEDICAL UNIVERSITY   (Japan)

^b Ikezawa Hospital   (Japan)

Author keywords

Adolescents; Autism spectrum disorders; Chromosome 15q11 13; Maternal uniparental disomy 15 (mUPD); Prader Willi syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; CHILD; CHILD PSYCHIATRY; CHROMOSOME 15Q; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPARATIVE STUDY; DISEASE ASSOCIATION; FEMALE; GENOTYPE; HUMAN; IMPULSIVENESS; INTELLIGENCE; JAPANESE (PEOPLE); MALE; PRADER WILLI SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOLOGIC ASSESSMENT; PSYCHOLOGICAL RATING SCALE; SCHOOL CHILD; SYMPTOMATOLOGY; UNIPARENTAL DISOMY; WECHSLER INTELLIGENCE SCALE; ASIAN CONTINENTAL ANCESTRY GROUP; GENE DELETION; GENETICS; INTELLIGENCE TEST; JAPAN;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; FEMALE; GENOTYPE; HUMANS; IMPULSIVE BEHAVIOR; INTELLIGENCE TESTS; JAPAN; MALE; PRADER-WILLI SYNDROME; SEQUENCE DELETION; UNIPARENTAL DISOMY;

EID: 84905901105     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36615     Document Type: Article

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