Diagnosis of 22q11.2 Deletion Syndrome in a Child With Congenital Heart Disease and Facial Dimorphism: A Case Report - Moura Carvalho, Natalia Dayane; Castillo Camargo, Ronaldo; Costa Garcia, Heliana Maria; Regina da Silva Teles, Suely; FANTIN, CLEITON (Acta Medica Iranica, 2021)