DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23

J Med Genet. 2003 Nov;40(11):832-6. doi: 10.1136/jmg.40.11.832.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Child
  • Chromosomes, Human, Pair 1 / genetics*
  • Female
  • Genes, Dominant / genetics*
  • Genes, Recessive / genetics
  • Genetic Linkage
  • Genetic Markers / genetics*
  • Haplotypes / genetics
  • Hearing Loss, Bilateral / diagnosis
  • Hearing Loss, Bilateral / genetics
  • Hearing Loss, Sensorineural / diagnosis
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Male
  • Pedigree
  • Physical Chromosome Mapping / methods*
  • Spain
  • Syndrome

Substances

  • Genetic Markers