2p15-p16.1 microdeletion syndrome: Molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

European Journal of Human Genetics

Volumn 19, Issue 12, 2011, Pages 1264-1270

  Liu, Xudong ^a,b,c   Malenfant, Patrick ^a,b,c   Reesor, Chelsea ^a,b,c   Lee, Alana ^a,b,c   Hudson, Melissa L ^a,b,c   Harvard, Chansonette ^d   Qiao, Ying ^c,d,e   Persico, Antonio M ^f,g   Cohen, Ira L ^c,h   Chudley, Albert E ^c,i   Forster Gibson, Cynthia ^a,c   Rajcan Separovic, Evica ^c,d   Lewis, Me Suzanne ^c,e   Holden, Jeanette J A ^a,b,c,j  

^a QUEEN S UNIVERSITY   (Canada)

^b Ongwanada Resource Centre   (Canada)

^c Autism Spectrum Disorders Canadian American Research Consortium   (United States)

^d UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^e UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^f UNIVERSITY CAMPUS BIO MEDICO   (Italy)

^g IRCCS FONDAZIONE SANTA LUCIA   (Italy)

^h NEW YORK STATE INSTITUTE FOR BASIC RESEARCH IN DEVELOPMENTAL DISABILITIES   (United States)

ⁱ UNIVERSITY OF MANITOBA   (Canada)

^j QUEEN S UNIVERSITY   (Canada)

more..

Author keywords

array comparative genomic hybridization; autism; exportin 1 gene; orthodenticle homolog 1 gene; real time quantitative PCR

Indexed keywords

EXPORTIN 1;

ARTICLE; AUTISM; CHROMOSOME 2P; COMMUNICATION DISORDER; COMPULSION; CONTROLLED STUDY; GENE; GENE DELETION; GENETIC ASSOCIATION; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MOLECULAR GENETICS; ORTHODENTICLE HOMOLOG 1 GENE; PRIORITY JOURNAL; SOCIAL INTERACTION; TERATOLOGY; UNITED STATES; VERBAL COMMUNICATION;

ALLELES; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOME BREAKPOINTS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 2; GENE ORDER; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; KARYOPHERINS; OTX TRANSCRIPTION FACTORS; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, CYTOPLASMIC AND NUCLEAR; SYNDROME;

EID: 81455154555     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2011.112     Document Type: Article

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