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Volumn 35, Issue 7, 2014, Pages 1742-1747

Neurodevelopmental outcome in Angelman syndrome: Genotype-phenotype correlations

Author keywords

15q11.2 q13; ADOS; Angelman syndrome; Autism; Intellectual disability; Language skills; Mullen

Indexed keywords

AGE; ARTICLE; AUTISM; CHILD; CHROMOSOME 15Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FOLLOW UP; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HAPPY PUPPET SYNDROME; HUMAN; LANGUAGE DEVELOPMENT; MALE; MENTAL DEVELOPMENT; NERVOUS SYSTEM DEVELOPMENT; UNIPARENTAL DISOMY; VISION; ANGELMAN SYNDROME; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHROMOSOME 15; DENMARK; DEVELOPMENTAL DISABILITIES; GENETIC ASSOCIATION; GENETICS; INTELLECTUAL DISABILITY; LANGUAGE DEVELOPMENT DISORDERS; NEUROPSYCHOLOGICAL TEST; PERCEPTUAL DISORDERS; PSYCHOMETRY; STATISTICS AND NUMERICAL DATA;

EID: 84899895541     PISSN: 08914222     EISSN: 18733379     Source Type: Journal    
DOI: 10.1016/j.ridd.2014.02.018     Document Type: Article
Times cited : (45)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.