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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

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author: Christopher A. Walsh  Gerard Berry  Leonard Rappaport  Children's Hospital Boston Genotype Phenotype Study Group  Shafali S Jeste  Eric M. Morrow  James F. Gusella  David T. Miller 

Publication date June 1, 2010
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