Molecular genetics of X-linked hearing impairment

Ann N Y Acad Sci. 1991:630:176-90. doi: 10.1111/j.1749-6632.1991.tb19586.x.
No abstract available

Publication types

  • Review

MeSH terms

  • Chromosome Mapping
  • Congenital Abnormalities / genetics
  • Deafness / genetics*
  • Female
  • Hearing Loss / genetics*
  • Humans
  • Male
  • Pedigree
  • Polymorphism, Restriction Fragment Length
  • Syndrome
  • X Chromosome*