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Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms

✍ Scribed by Shashi, Vandana; Francis, Alan; Hooper, Stephen R; Kranz, Peter G; Zapadka, Michael; Schoch, Kelly; Ip, Edward; Tandon, Neeraj; Howard, Timothy D; Keshavan, Matcheri S

Book ID: 120612962
Publisher: Nature Publishing Group
Year: 2012
Tongue: English
Weight: 418 KB
Volume: 20
Category: Article
ISSN: 1018-4813
DOI: 10.1038/ejhg.2012.138

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## Abstract In this article, I present an updated account that attempts to explain, in cognitive processing and neural terms, the nonverbal intellectual impairments experienced by most children with deletions of chromosome 22q11.2. Specifically, I propose that this genetic syndrome leads to early d