Disease | heart disease |
Phenotype | C0012236|22q11.2 deletion syndrome |
Sentences | 3 |
PubMedID- 25317860 | Background: to alert for the diagnosis of the 22q11.2 deletion syndrome (22q11.2ds) in patients with congenital heart disease (chd). |
PubMedID- 24880467 | Molecular screening for 22q11.2 deletion syndrome in patients with congenital heart disease. |
PubMedID- 24596813 | Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome. |
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