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Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
Common genetic variants, acting additively, are a major source of risk for autism
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects
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