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Article

The development of cognitive control in children with chromosome 22q11.2 deletion syndrome

10 Jun 2014

Abstract excerpt

Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, and it is associated with cognitive impairments across many domains. While impairments in cognitive control have been described in children with 22q11.2DS, the nature and development of these impairments are not clear. Children with 22q11.2DS and typically developing children (TD) were tested on four well-validated...

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Identifiers

PMID: 24959159
DOI: 10.3389/fpsyg.2014.00566

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