Article

Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications

2023-12-29

Abstract excerpt

<title>Abstract</title> <p>Rare recurrent copy number variants (CNVs) at chromosomal loci 22q11.2 and 16p11.2 are among the most common rare genetic disorders associated with significant risk for neuropsychiatric disorders across the lifespan. Microdeletions and duplications in these loci are associated with neurocognitive deficits, yet there are few studies comparing these groups using the same measures. We addr...

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Literature Corpus work: 332d5d3d-74e1-5954-87a1-103f90536933
DOI: 10.21203/rs.3.rs-3393845/v1

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