Browsing by Subject "22q11.2 deletion syndrome"

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    • Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease 
      Butcher, Nancy J.; Marras, Connie; Pondal, Margarita; Rusjan, Pablo; Boot, Erik; Christopher, Leigh; Repetto, Gabriela M.; Fritsch, Rosemarie; Chow, Eva W.C.; Masellis, Mario; Strafella, Antonio P.; Lang, Anthony E.; Bassett, Anne S. (Oxford University Press, 2017)
      © The Author (2017). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved.The recurrent 22q11.2 deletion is a genetic risk factor for early-onset Parkinson's disease. Adults with ...
    • Psychiatric manifestations of 22q11.2 deletion syndrome: a literature review 
      Bertrán, M.; Tagle, F. P.; Irarrázaval Domínguez, Matías (Elsevier, 2018)
      Introduction: The 22q11.2 deletion syndrome is a genetic disorder with variable clinical manifestations. It affects one out of 5950 neonates and has an autosomal dominant inheritance pattern. The aim of this article is to ...