Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk

PLoS ONE

Volumn 6, Issue 10, 2011, Pages

  Salyakina, Daria ^a   Cukier, Holly N ^a   Lee, Joycelyn M ^a   Sacharow, Stephanie ^a   Nations, Laura D ^a   Ma, Deqiong ^a   Jaworski, James M ^a   Konidari, Ioanna ^a   Whitehead, Patrice L ^a   Wright, Harry H ^b   Abramson, Ruth K ^b   Williams, Scott M ^c   Menon, Ramkumar ^d   Haines, Jonathan L ^c   Gilbert, John R ^a   Cuccaro, Michael L ^a   Pericak Vance, Margaret A ^a  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF SOUTH CAROLINA SCHOOL OF MEDICINE   (United States)

^c VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^d EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTISM; CHILD; CHL1 GENE; CONTROLLED STUDY; COPY NUMBER VARIATION; EXTENDED FAMILY; FEMALE; FGFBP3 GENE; GENE; GENE DELETION; GENE DISRUPTION; GENE DUPLICATION; GENETIC ASSOCIATION; GENOTYPE; HUMAN; HUMAN GENOME; ICA1 GENE; MAJOR CLINICAL STUDY; MALE; NXPH1 GENE; PATHOGENESIS; POUF41 GENE; PRESCHOOL CHILD; SCHIZOPHRENIA; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE;

ADOLESCENT; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; PEDIGREE; YOUNG ADULT;

EID: 80053892695     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0026049     Document Type: Article

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