Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3

Adv Otorhinolaryngol. 2000:56:158-63. doi: 10.1159/000059096.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 21*
  • Deafness / genetics*
  • Female
  • Genes, Recessive
  • Humans
  • Male
  • Pedigree