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Results 1 - 2 of 2 for Conotruncal anomaly face syndrome
  1. 22q11.2 deletion syndrome 
    ... syndrome, velocardiofacial syndrome (also called Shprintzen syndrome), and conotruncal anomaly face syndrome. In addition, some children with the 22q11.2 ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  2. TBX1 gene 
    ... or Free article on PubMed Central Baldini A. DiGeorge syndrome: an update. Curr Opin Cardiol. 2004 May;19( ... localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation. Hum Mol Genet. ...
    https://medlineplus.gov/genetics/gene/tbx1 - Genetics