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November 20, 2001Circulation

NKX2.5 Mutations in Patients With Tetralogy of Fallot

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EGElizabeth GoldmuntzChildren's Hospital of PhiladelphiaEGElizabeth A. GeigerUniversity of Colorado DenverDBD. Woodrow BensonPediatric / Congenital Cardiology

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Goldmuntz et al. (2001) studied this question.

synapsesocial.com/papers/6a8a700a9be9d02581bdaec9https://doi.org/10.1161/hc4601.098427
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Chromosome 22q11 microdeletions in tetralogy of Fallot.1996 · 53 citations
  2. 2Frequency of 22q11 deletions in patients with conotruncal defects1998 · 596 citations
  3. 3CONGENITAL HEART DISEASE: PREVALENCE AT LIVEBIRTH1985 · 1,030 citations
  4. 4Congenital Heart Disease Caused by Mutations in the Transcription Factor <i>NKX2-5</i>1998 · 1,311 citations
  5. 5Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease2000 · 166 citations