22q11.2 deletion detected by in situ hybridization in Mexican patients with velocardiofacial syndrome-like features
Colomb. med; 49 (3), 2018
Abstract Introduction: Deletion 22q11.2 occurs in 1:4,000-1:6,000 live births while 10p13p14 deletion is found in 1:200,000 newborns. Both deletions have similar clinical features such as congenital heart disease and immunological anomalies. Objective: We looked for a 22q11.2 deletion in Mexican patien...
Síndrome de DiGeorge/diagnóstico, Cardiopatías Congénitas/diagnóstico, Hibridación Fluorescente in Situ, Tetralogía de Fallot/diagnóstico, Análisis Citogenético, Síndrome de DiGeorge/genética, Síndrome de DiGeorge/fisiopatología, Cardiopatías Congénitas/genética, Defectos del Tabique Interventricular/diagnóstico, Defectos del Tabique Interventricular/genética, México, Estudios Prospectivos, Tetralogía de Fallot/genética