Confirmation of the location of a Waardenburg syndrome type I mutation on human chromosome 2q. Tight linkage to FN1 and ALPP

Ann N Y Acad Sci. 1991:630:295-7. doi: 10.1111/j.1749-6632.1991.tb19611.x.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Southern
  • Chromosome Mapping
  • Chromosomes, Human, Pair 2*
  • Chromosomes, Human, Pair 3
  • DNA / genetics
  • DNA / isolation & purification
  • Deafness / genetics*
  • Female
  • Genetic Linkage*
  • Genetic Markers
  • Humans
  • Male
  • Mutation*
  • Pedigree
  • Polymorphism, Restriction Fragment Length
  • Waardenburg Syndrome / genetics*

Substances

  • Genetic Markers
  • DNA