ArticleHeart (British Cardiac Society)1996
Isomerism of the atrial appendages associated with 22q11 deletion in a fetus.
Article in Heart (British Cardiac Society), 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed, 23 citations in OpenAlex.
- Transcription factor pathways and congenital heart disease.Current topics in developmental biology · 2012Review
- Prenatal diagnosis of complete atrioventricular septal defect: perinatal and neonatal outcomes.Obstetrics and gynecology international · 2009Article
- A population study of chromosome 22q11 deletions in infancy.Archives of disease in childhood · 1998Article
- Prenatal diagnosis of 22q11 deletions: a series of five cases with congenital heart defects.Journal of medical genetics · 1997Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
There is a strong association between prenatally diagnosed structural heart disease and fetal chromosomal abnormalities. Isomerism of the atrial appendages is an exception to this because the fetal karyotype is usually normal in this condition. A case of atrial isomerism diagnosed antenatally with a normal female karyotype but with a microdeletion of chromosome 22q11 is reported.
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