Genotype-phenotype association studies of chromosome 8p inverted duplication deletion syndrome

Behavior Genetics

Volumn 41, Issue 3, 2011, Pages 373-380

  Fisch, Gene S ^a   Davis, Ryan ^b   Youngblom, Janey ^c   Gregg, Jeff ^b  

^a NEW YORK UNIVERSITY   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c CALIFORNIA STATE UNIVERSITY   (United States)

Author keywords

Autism; CGH microarray; Intellectual disability; Inverted duplication deletion 8p21 23; Subtelomeric deletion

Indexed keywords

ADAPTIVE BEHAVIOR; ADOLESCENT; ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; CASE REPORT; CHILD; CHROMOSOME 8P INVERTED DUPLICATION DELETION SYNDROME; CHROMOSOME DISORDER; CHROMOSOME DUPLICATION; COGNITIVE DEFECT; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; CYTOGENETICS; DISEASE ASSOCIATION; DISEASE SEVERITY; FEMALE; GENE DELETION; GENE LOCUS; GENE OVEREXPRESSION; GENETIC ASSOCIATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; INTELLECTUAL IMPAIRMENT; MALE; MENTAL INSTABILITY; PRESCHOOL CHILD;

ADOLESCENT; AFFECTIVE SYMPTOMS; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CHILD; CHILD BEHAVIOR DISORDERS; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOMES, HUMAN, PAIR 8; COGNITION DISORDERS; FEMALE; GENE EXPRESSION; GENOTYPE; HUMANS; LONGITUDINAL STUDIES; MALE; NEUROPSYCHOLOGICAL TESTS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE; SYNDROME; TRISOMY;

EID: 79958188547     PISSN: 00018244     EISSN: 15733297     Source Type: Journal    
DOI: 10.1007/s10519-011-9447-4     Document Type: Article

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