Article

Language and communication deficits in Chromosome 16p11.2 Deletion Syndrome

2022-03-12

Abstract excerpt

<p>Chromosome 16p11.2 Deletion Syndrome (OMIM #611913) is a rare genetic condition resulting from the partial deletion of approximately 25 genes at chromosome 16. Affected people exhibit a variable clinical profile, featuring developmental and language delay, mild intellectual disability (ID), motor problems, social deficits and some autism spectrum disorders (ASD) traits, and mild dysmorphisms. A precise characte...

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Literature Corpus work: e05e93e6-c9ca-5982-a0e1-8a6e39c2fd69
DOI: 10.31234/osf.io/dtcy2

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