Sensorineural hearing impairment, non-syndromic: DFNB5, 6, 7. Homozygosity mapping to localize genes causing autosomal recessive non-syndromic hearing loss

Adv Otorhinolaryngol. 2000:56:152-7. doi: 10.1159/000059103.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Chromosome Mapping*
  • Chromosomes, Human, Pair 14
  • Chromosomes, Human, Pair 7
  • Chromosomes, Human, Pair 9
  • Deafness / genetics*
  • Genes, Recessive
  • Hearing Loss, Sensorineural / genetics*
  • Homozygote
  • Humans