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Conotruncal defect
- 22q11.2 Deletion Syndrome (DiGeorge Syndrome) (For Parents) (Nemours Foundation)... condition, DiGeorge syndrome, velocardiofacial syndrome (VCFS), Shprintzen syndrome, conotruncal anomaly face syndrome, Caylor cardiofacial syndrome, genetic, inherited, ...
- Congenital Heart Defects/Specifics ... Congenital Heart Defects