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A large data resource of genomic copy number variation across neurodevelopmental disorders

https://doi.org/10.1038/s41525-019-0098-3

50/50 checkable references clean · checked 2026-07-23

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

The 50 checked references that resolve

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Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family

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Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects

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Clinically relevant copy number variations detected in cerebral palsy

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