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January 1, 1996Archives of Disease in ChildhoodOpen Access

Chromosome 22q11 microdeletions in tetralogy of Fallot.

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Authors

ATAlison H. TrainerThe University of MelbourneNMNorma MorrisonSouthern General HospitalADAdam DunlopDrexel University

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Cite This Study

Trainer et al. (1996) studied this question.

synapsesocial.com/papers/6a71f51578a11c550e0be1f2https://doi.org/10.1136/adc.74.1.62
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Also Consider

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

  1. 1DiGeorge syndrome: part of CATCH 22.1993 · 511 citations
  2. 2Tetralogy of Fallot1992 · 19 citations
  3. 3A family study of Fallot's tetralogy.1972 · 38 citations
  4. 4Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.1993 · 490 citations
  5. 5Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.1993 · 225 citations