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Volumn 77, Issue 9, 2015, Pages 785-793

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population

(25)  Hanson, Ellen a,b   Bernier, Raphael c   Porche, Ken a   Jackson, Frank I a   Goin Kochel, Robin P d   Snyder, Leeanne Green a   Snow, Anne V a,b   Wallace, Arianne Stevens c   Campe, Katherine L a   Zhang, Yuan e   Chen, Qixuan e   D'Angelo, Debra e   Moreno De Luca, Andres f   Orr, Patrick T f   Boomer, K B g   Evans, David W f   Kanne, Stephen h   Berry, Leandra d   Miller, Fiona K a   Olson, Jennifer a   more..


Author keywords

16p11.2 Deletion; Autism; Autism spectrum disorder; Developmental disability; Genetics; Psychiatric diagnosis

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME 16P; CHROMOSOME DELETION; COMPULSION; CONTROLLED STUDY; DEVELOPMENTAL COORDINATION DISORDER; DEVELOPMENTAL DISORDER; DSM-IV; FEMALE; HANDEDNESS; HUMAN; INTELLIGENCE; INTELLIGENCE QUOTIENT; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; MALE; MENTAL DISEASE; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; SOCIAL INTERACTION; SPEECH DISORDER; SPEECH SOUND DISORDER; CHROMOSOME 16; COGNITION; GENETICS; HETEROZYGOTE; PATHOPHYSIOLOGY; PRESCHOOL CHILD; PSYCHOLOGY; YOUNG ADULT;

EID: 84926373318     PISSN: 00063223     EISSN: 18732402     Source Type: Journal    
DOI: 10.1016/j.biopsych.2014.04.021     Document Type: Article
Times cited : (186)

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