Malgorzata J.M. Nowaczyk

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PURPOSE The purpose of the current study was to assess the penetrance of NRXN1 deletions. METHODS We compared the prevalence and genomic extent of NRXN1 deletions identified among 19,263 clinically referred cases to that of 15,264 controls. The burden of additional clinically relevant copy-number variations (CNVs) was used as a proxy to estimate the(More)
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