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Browsing by Subject "22q11.2 deletion syndrome"

Browsing by Subject "22q11.2 deletion syndrome"

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  • Butcher, Nancy; Marras, Connie; Pondal, Margarita; Rusjan, Pablo; Boot, Erik; Christopher, Leigh; Repetto, Gabriela; Fritsch, Rosemarie; Chow, Eva; Masellis, Mario; Strafella, Antonio; Lang, Anthony; Bassett, Anne (Oxford University Press, 2017)
    The recurrent 22q11.2 deletion is a genetic risk factor for early-onset Parkinson's disease. Adults with the associated 22q11.2 deletion syndrome (22q11.2DS) may exhibit phenotypes that could help identify those at highest ...

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