ArticleJournal of medical genetics1994
Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21.
Article in Journal of medical genetics, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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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, 4 citations in OpenAlex.
- Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysis.Human genetics · 1995Article
- Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindred.Human genetics · 1995Article
- Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families.Journal of medical genetics · 1994Article
- Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis.Journal of medical genetics · 1994Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The three microsatellite repeat loci, DXS986, DXS995, and DXS1002, have been mapped to Xq13.2-21.1. We report here their relative order and their localisation within Xq21. These loci will be useful for the genetic mapping of disease loci in this region, in particular X linked deafness, as DXS995 lies in the region critical for this disorder.
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Registered trials
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