Rare deletions at the neurexin 3 locus in autism spectrum disorder

American Journal of Human Genetics

Volumn 90, Issue 1, 2012, Pages 133-141

  Vaags, Andrea K ^a   Lionel, Anath C ^a,b   Sato, Daisuke ^a   Goodenberger, McKinsey ^c   Stein, Quinn P ^d   Curran, Sarah ^e   Ogilvie, Caroline ^e   Ahn, Joo Wook ^e   Drmic, Irene ^f   Senman, Lili ^f   Chrysler, Christina ^g   Thompson, Ann ^g   Russell, Carolyn ^g   Prasad, Aparna ^a   Walker, Susan ^a   Pinto, Dalila ^a   Marshall, Christian R ^a   Stavropoulos, Dimitri J ^f   Zwaigenbaum, Lonnie ^h   Fernandez, Bridget A ⁱ   Fombonne, Eric ^j   Bolton, Patrick F ^e   Collier, David A ^e   Hodge, Jennelle C ^c   Roberts, Wendy ^f,k   Szatmari, Peter ^g   Scherer, Stephen W ^a,b   more..

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c MAYO CLINIC   (United States)

^d UNIVERSITY OF SOUTH DAKOTA   (United States)

^e KING'S COLLEGE LONDON   (United Kingdom)

^f HOSPITAL FOR SICK CHILDREN   (Canada)

^g MCMASTER UNIVERSITY   (Canada)

^h UNIVERSITY OF ALBERTA   (Canada)

ⁱ MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

^j MONTREAL CHILDREN S HOSPITAL   (Canada)

^k University of Toronto   (Canada)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTISM; COPY NUMBER VARIATION; GENE; GENE DELETION; GENE LOCUS; GENE MUTATION; HUMAN; NEUREXIN 1 GENE; NEUREXIN 2 GENE; NEUREXIN 3 GENE; PRIORITY JOURNAL; SYNAPSE;

ADOLESCENT; ADULT; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 14; DNA COPY NUMBER VARIATIONS; FEMALE; GENE DELETION; GENETIC LOCI; HUMANS; MALE; NERVE TISSUE PROTEINS; PEDIGREE; PENETRANCE; YOUNG ADULT;

EID: 84855829221     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2011.11.025     Document Type: Article

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