ArticleInternational journal of legal medicine2019
Non-pathological complete paternal uniparental isodisomy of chromosome 2 revealed in a maternity testing case.
Article in International journal of legal medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 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
5 citing papers in PubMed, 12 citations in OpenAlex.
- Case reports on uniparental disomy of chromosomes 6 and 3 in paternity testing.Forensic sciences research · 2024Article
- Maternal Uniparental Isodisomy of Chromosome 2 Leading to Homozygous Variants inGlobal medical genetics · 2024Review
- Article
- A case of 46,XX/46,XX chimerism in a phenotypically normal woman.International journal of legal medicine · 2020Article
- Multiple methods used for type detection of uniparental disomy in paternity testing.International journal of legal medicine · 2020Article
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Authors and funding
11 authors at 5 institutions in 1 country.
Funding
Abstract
We present a duo paternity test case to assess the biological relationship between a woman and her female child. After analyzing 57 autosomal and 19 X-chromosomal short tandem repeat loci, mother-daughter exclusions were discovered at four loci, which were all located on chromosome 2. Further testing of whole-genome single nucleotide polymorphisms confirmed that the daughter had complete uniparental disomy (UPD) of chromosome 2. This study presents a cautionary case demonstrating that hasty decisions of parentage exclusion should not be made when genetic markers on the same chromosome do not conform to Mendel's laws due to UPD.
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Registered trials
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