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Lett."},{"key":"key\n\t\t\t\t20170522135828_DDS111C82","doi-asserted-by":"crossref","first-page":"199","DOI":"10.1016\/j.ajhg.2007.09.011","article-title":"Disruption of neurexin 1 associated with autism spectrum disorder","volume":"82","year":"2008","journal-title":"Am. J. Hum. Genet."},{"key":"key\n\t\t\t\t20170522135828_DDS111C83","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1016\/j.ajhg.2007.12.009","article-title":"Structural variation of chromosomes in autism spectrum disorder","volume":"82","year":"2008","journal-title":"Am. J. Hum. Genet."},{"key":"key\n\t\t\t\t20170522135828_DDS111C84","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1038\/ng1985","article-title":"Mapping autism risk loci using genetic linkage and chromosomal rearrangements","volume":"39","year":"2007","journal-title":"Nat. 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Genet."},{"key":"key\n\t\t\t\t20170522135828_DDS111C88","first-page":"458","article-title":"Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia","volume":"17","year":"2008","journal-title":"Hum. Mol. Genet."},{"key":"key\n\t\t\t\t20170522135828_DDS111C89","doi-asserted-by":"crossref","first-page":"988","DOI":"10.1093\/hmg\/ddn351","article-title":"Disruption of the neurexin 1 gene is associated with schizophrenia","volume":"18","year":"2009","journal-title":"Hum. Mol. Genet."},{"key":"key\n\t\t\t\t20170522135828_DDS111C90","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1186\/1744-9081-7-7","article-title":"A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population","volume":"7","year":"2011","journal-title":"Behav. Brain Funct."},{"key":"key\n\t\t\t\t20170522135828_DDS111C91","doi-asserted-by":"crossref","first-page":"387","DOI":"10.1016\/j.neuron.2007.04.015","article-title":"Behavioral phenotypes of Disc1 missense mutations in mice","volume":"54","year":"2007","journal-title":"Neuron"},{"key":"key\n\t\t\t\t20170522135828_DDS111C92","doi-asserted-by":"crossref","first-page":"585","DOI":"10.1038\/mp.2010.134","article-title":"Synaptic modulators Nrxn1 and Nrxn3 are disregulated in a Disc1 mouse model of schizophrenia","volume":"16","year":"2011","journal-title":"Mol. 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