Journal article
Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis
American journal of medical genetics, Vol.51(2), pp.176-184
06/01/1994
DOI: 10.1002/ajmg.1320510222
PMID: 8092199
Abstract
Branchiootorenal (BOR) syndrome is a common autosomal dominant form of hearing impairment previously mapped to 8q. This report refines the localization of the BOR syndrome gene by haplotype analysis to the interval flanked by markers D8S553 and D8S286. By multipoint linkage analysis, the disease locus most likely is flanked by markers D8S530 and D8S279. © 1994 Wiley‐Liss, Inc.
Details
- Title: Subtitle
- Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis
- Creators
- Li NiMichael J WagnerWilliam J KimberlingMarcus E PembreyKenneth M GrundfastShrawan KumarStephen P DaigerDan E WellsKristin JohnsonRichard J. H Smith
- Resource Type
- Journal article
- Publication Details
- American journal of medical genetics, Vol.51(2), pp.176-184
- DOI
- 10.1002/ajmg.1320510222
- PMID
- 8092199
- NLM abbreviation
- Am J Med Genet
- ISSN
- 0148-7299
- eISSN
- 1096-8628
- Publisher
- Wiley; New York
- Number of pages
- 9
- Language
- English
- Date published
- 06/01/1994
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
- Record Identifier
- 9984007186502771
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