Human genetic mapping and inherited deafness syndromes

Ann N Y Acad Sci. 1991:630:38-48. doi: 10.1111/j.1749-6632.1991.tb19574.x.
No abstract available

Publication types

  • Review

MeSH terms

  • Alleles
  • Chromosome Mapping
  • Chromosomes, Human, Pair 10*
  • Deafness / genetics*
  • Humans
  • Mutation
  • Software
  • Syndrome