Abnormalities in gray matter microstructure in young adults with 22q11.2 deletion syndrome

Abnormalities in gray matter microstructure in young adults with 22q11.2 deletion syndrome

Background: 22q11.2 Deletion Syndrome (22q11DS) is a genetic, neurodevelopmental disorder characterized by a chromosomal deletion and a distinct cognitive profile. Although abnormalities in the macrostructure of the cortex have been identified in individuals with 22q11DS, it is not known if there ar...

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Main Authors: Zora Kikinis, Nikos Makris, Valerie J. Sydnor, Sylvain Bouix, Ofer Pasternak, Ioana L. Coman, Kevin M. Antshel, Wanda Fremont, Marek R. Kubicki, Martha E. Shenton, Wendy R. Kates, Yogesh Rathi
Format: Article
Language:English
Published: Elsevier 2019-01-01
Series:NeuroImage: Clinical
Online Access:http://www.sciencedirect.com/science/article/pii/S2213158218303644

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http://www.sciencedirect.com/science/article/pii/S2213158218303644

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