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JAG1 Mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot
Authors:Maria Cristina Digilio  Alessandro De Luca  Francesca Lepri  Valentina Guida  Rosangela Ferese  Maria Lisa Dentici  Adriano Angioni  Bruno Marino  Bruno Dallapiccola
Affiliation:1. Medical Genetics and Cytogenetics, Bambino Gesù Children's Hospital, IRCCS, , Rome, Italy;2. Mendel Laboratory, Casa Sollievo Della Sofferenza Hospital, IRCCS, , San Giovanni Rotondo, Italy;3. Pediatric Cardiology, Department of Pediatrics, Roma‐Sapienza University, and Lorillard Spencer Cenci Foundation, , Rome, Italy
Abstract:
Keywords:deletion 22q11.2  DiGeorge/Velo‐Cardio‐Facial syndrome  Alagille syndrome  JAG1 gene  tetralogy of Fallot
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