A progress report on the localization of Usher syndrome type II to chromosome 1q

Ann N Y Acad Sci. 1991:630:284-7. doi: 10.1111/j.1749-6632.1991.tb19606.x.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 1*
  • Deafness / genetics*
  • Genetic Linkage
  • Genetic Markers
  • Humans
  • Lod Score
  • Recombination, Genetic
  • Retinitis Pigmentosa / genetics*
  • Software
  • Syndrome

Substances

  • Genetic Markers