Ontology highlight
ABSTRACT:
SUBMITTER: Tylee DS
PROVIDER: S-EPMC5522376 | biostudies-literature | 2017
REPOSITORIES: biostudies-literature
Tylee Daniel S DS Kikinis Zora Z Quinn Thomas P TP Antshel Kevin M KM Fremont Wanda W Tahir Muhammad A MA Zhu Anni A Gong Xue X Glatt Stephen J SJ Coman Ioana L IL Shenton Martha E ME Kates Wendy R WR Makris Nikos N
NeuroImage. Clinical 20170511
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a genetic neurodevelopmental syndrome that has been studied intensively in order to understand relationships between the genetic microdeletion, brain development, cognitive function, and the emergence of psychiatric symptoms. White matter microstructural abnormalities identified using diffusion tensor imaging methods have been reported to affect a variety of neuroanatomical tracts in 22q11.2DS. In the present study, we sought to combine two dis ...[more]