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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Publicado en:Neuroimage Clin
Autores principales: Kikinis, Zora, Makris, Nikos, Sydnor, Valerie J., Bouix, Sylvain, Pasternak, Ofer, Coman, Ioana L., Antshel, Kevin M., Fremont, Wanda, Kubicki, Marek R., Shenton, Martha E., Kates, Wendy R., Rathi, Yogesh
Formato: Artigo
Lenguaje:Inglês
Publicado: Elsevier 2018
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6411601/
https://ncbi.nlm.nih.gov/pubmed/30522971
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2018.101611
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