Open AccessIncreased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms
Author(s) -
Vandana Shashi,
Alan Francis,
Stephen R. Hooper,
Peter G. Kranz,
Michael E. Zapadka,
Kelly Schoch,
Edward H. Ip,
Neeraj Tandon,
Timothy D. Howard,
Matcheri S. Keshavan
Publication year - 2012
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/g3pb-c916
Subject(s) - neurocognitive , corpus callosum , deletion syndrome , genetic syndromes , chromosome , genetics , medicine , psychology , biology , neuroscience , pediatrics , pathology , cognition , gene , phenotype