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Volumn 21, Issue 21, 2012, Pages 4781-4792

Individual common variants exert weak effects on the risk for autism spectrum disorders

(137)  Anney, Richard a   Klei, Lambertus b   Pinto, Dalila c,ad   Almeida, Joana d   Bacchelli, Elena e   Baird, Gillian f   Bolshakova, Nadia a   Bölte, Sven g   Bolton, Patrick F h   Bourgeron, Thomas i,j   Brennan, Sean a   Brian, Jessica k   Casey, Jillian l   Conroy, Judith l   Correia, Catarina m,n   Corsello, Christina o   Crawford, Emily L p   De jonge, Maretha r   Delorme, Richard s   Duketis, Eftichia g   more..


Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTISM; CNTNAP2 GENE; CONTROLLED STUDY; GENE; GENE FREQUENCY; GENETIC VARIABILITY; HUMAN; LANGUAGE DEVELOPMENT; MASSETER MUSCLE; PHENOTYPE; PREDICTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84867829870     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/dds301     Document Type: Article
Times cited : (303)

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