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PedAM

Pediatric Disease Annotations & Medicines




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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