D. Cao

22q11.2 microdeletion and immunological status of Vietnamese children with tetralogy of Fallot and pulmonary atresia with ventricular septal defect

The 22q11.2 deletion (22q11.2Del) is one of the most common chromosomal microdeletions associated with a broad range of clinical manifestations, including congenital heart disease and immunodeficiency. Several studies reported a high frequency of 22q11.2Del in patients with conot...