Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems

Genetics in Medicine

Volumn 13, Issue 10, 2011, Pages 868-880

  Sahoo, Trilochan ^a   Theisen, Aaron ^a   Rosenfeld, Jill A ^a   Lamb, Allen N ^a   Ravnan, J Britt ^a   Schultz, Roger A ^a   Torchia, Beth S ^a   Neill, Nicholas ^a   Casci, Ian ^a   Bejjani, Bassem A ^a   Shaffer, Lisa G ^a  

^a PerkinElmer   (United States)

Author keywords

CNV; deletion; duplication; microarray; neurodevelopment

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BEHAVIOR DISORDER; CHILD; CHROMOSOME 15Q; CHROMOSOME 16P; CHROMOSOME 1Q; CHROMOSOME 22Q; COPY NUMBER VARIATION; GENE LOCUS; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; INFANT; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MICROARRAY ANALYSIS; PRESCHOOL CHILD; SCHIZOPHRENIA; SCHOOL CHILD; SPEECH DISORDER;

ADOLESCENT; BEHAVIORAL SYMPTOMS; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOMES, HUMAN; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISABILITIES; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; HEREDITY; HUMANS; INFANT; INFANT, NEWBORN; LANGUAGE DEVELOPMENT DISORDERS; MALE; SCHIZOPHRENIA; YOUNG ADULT;

EID: 80053903662     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1097/GIM.0b013e3182217a06     Document Type: Article

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