Search Results - Costa Garcia, Heliana Maria

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    Diagnosis of 22q11.2 Deletion Syndrome in a Child With Congenital Heart Disease and Facial Dimorphism: A Case Report

    Diagnosis of 22q11.2 Deletion Syndrome in a Child With Congenital Heart Disease and Facial Dimorphism: A Case Report by Moura Carvalho, Natalia Dayane, Camargo, Ronaldo Castillo, Costa Garcia, Heliana Maria, Silva Teles, Suely Regina da, Fantin, Cleiton

    Published in Acta medica Iranica
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