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    • 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 ...