Browsing HMS Scholarly Articles by Keyword "22q11.2 deletion syndrome (22q11.2DS,CFS)"

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    • Genetic contributions to changes of fiber tracts of ventral visual stream in 22q11.2 deletion syndrome 

      Kikinis, Zora; Makris, Nikos; Finn, Christine; Bouix, Sylvain; Lucia, Diandra; Coleman, Michael James; Tworog-Dube, Erica; Kikinis, Ron; Kucherlapati, Raju; Shenton, Martha Elizabeth; Kubicki, Marek R. (Springer Science + Business Media, 2013)
      Patients with 22q11.2 deletion syndrome (22q11.2DS) represent a population at high risk for developing schizophrenia, as well as learning disabilities. Deficits in visuo-spatial memory are thought to underlie some of the ...