A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci

J Med Genet. 2004 Feb;41(2):e14. doi: 10.1136/jmg.2003.012500.
No abstract available

Publication types

  • Comparative Study
  • Letter
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Animals
  • Child
  • Chromosomes, Human, Pair 7 / genetics*
  • Conserved Sequence / genetics
  • Female
  • Genes, Dominant / genetics*
  • Genetic Linkage / genetics
  • Genetic Markers / genetics*
  • Genotype
  • Haplotypes / genetics
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Male
  • Mice
  • Pedigree
  • Physical Chromosome Mapping*
  • Synteny / genetics

Substances

  • Genetic Markers