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December 1, 1996HeartOpen Access

Isomerism of the atrial appendages associated with 22q11 deletion in a fetus.

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Authors

RYRobert YatesGreat Ormond Street HospitalFRF. Lucy RaymondUniversity of CambridgeACAndrew C. CookUniversity College London

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Yates et al. (1996) studied this question.

synapsesocial.com/papers/6a94841961244928ec0100edhttps://doi.org/10.1136/hrt.76.6.548
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Also Consider

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

  1. 1Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.1993 · 225 citations
  2. 2Syndromes of asplenia and polysplenia. A review of cardiac and non-cardiac malformations in 60 cases withspecial reference to diagnosis and prognosis.1975 · 372 citations
  3. 3Atrioventricular septal defect in fetal life—a clinicopathological correlation1991 · 10 citations
  4. 4Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.1993 · 489 citations
  5. 5Mutations of the<i>Connexin43</i>Gap-Junction Gene in Patients with Heart Malformations and Defects of Laterality1995 · 382 citations