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Browsing by Subject "22q11 Deletion Syndrome/diagnosis"

Browsing by Subject "22q11 Deletion Syndrome/diagnosis"

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  • Guzman, Maria; Delgado, Iris; Lay-Son, Guillermo; Williams, Edward; Puga, Alonso; Repetto, Gabriela (John Wiley & Sons, 2012)
    Chromosome 22q11 microdeletion syndrome has a wide range of clinical manifestations including congenital heart malformations, palatal defects, endocrine abnormalities, immunologic deficits, learning difficulties, and an ...

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