Article

Communication deficits in a case of 22q11.23 Duplication Syndrome with a deletion in 7q31 encompassing FOXP2

2021-03-22

Abstract excerpt

<p>Copy number variants (CNVs) found in individuals with communication deficits provide a valuable window to the genetic causes of problems with language and more generally, to the genetic foundation of the human-specific ability to learn and use languages. In this paper, we report in detail on the language and communication problems of a patient with a microduplication in 22q11.23 and a microdeletion in 7q31 enco...

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Literature Corpus work: 7ca1248b-3fc0-58b7-b443-1e7d8d3e8d0f
DOI: 10.31234/osf.io/3nme8

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