Deafness Locus DFNB16 Is Located on Chromosome 15q13-q21 within a 5-cM Interval Flanked by Markers D15S994 and D15S132
- 1 April 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (4) , 1238-1241
- https://doi.org/10.1086/302321
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.Journal of Medical Genetics, 1997
- Report of the Third International Workshop on Human Chromosome 15 Mapping 1996Cytogenetic and Genome Research, 1997
- A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22Human Molecular Genetics, 1996
- A comprehensive genetic map of the human genome based on 5,264 microsatellitesNature, 1996
- A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) geneHuman Molecular Genetics, 1995