CHD8 intragenic deletion associated with autism spectrum disorder

European Journal of Medical Genetics

Volumn 59, Issue 4, 2016, Pages 189-194

  Stolerman, Elliot S ^a   Smith, Brooke ^a   Chaubey, Alka ^a   Jones, Julie R ^a  

^a GREENWOOD GENETIC CENTER   (United States)

Author keywords

ASD; Autism; Autism spectrum disorders; CHD8

Indexed keywords

CHROMODOMAIN HELICASE DNA BINDING PROTEIN 8; DNA BINDING PROTEIN; UNCLASSIFIED DRUG; CHD8 PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

ANGER; ARTICLE; AUTISM; CASE REPORT; CHILD; COMPULSION; DEVELOPMENTAL DISORDER; DISRUPTIVE BEHAVIOR; DNA METHYLATION; EXON; FAMILY HISTORY; FOLLOW UP; GENE; GENE DELETION; GENETIC ASSOCIATION; GENETIC SCREENING; HAPPY PUPPET SYNDROME; HUMAN; KARYOTYPE; LANGUAGE DELAY; MALE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NEXT GENERATION SEQUENCING; OCCUPATIONAL THERAPY; PHYSICAL EXAMINATION; PHYSIOTHERAPY; PICA; PRADER WILLI SYNDROME; RISK FACTOR; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SPEECH THERAPY; GENETICS; MUTATION; PATHOLOGY;

AUTISM SPECTRUM DISORDER; CHILD; DEVELOPMENTAL DISABILITIES; DNA-BINDING PROTEINS; EXONS; GENE DELETION; HUMANS; MALE; MUTATION; TRANSCRIPTION FACTORS;

EID: 84959486708     PISSN: 17697212     EISSN: 18780849     Source Type: Journal    
DOI: 10.1016/j.ejmg.2016.02.010     Document Type: Article

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