Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome

Trans Am Ophthalmol Soc. 1989:87:658-728.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Adult
  • Aged
  • Cataract / congenital
  • Cataract / genetics*
  • Child
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 22*
  • Corneal Diseases / genetics*
  • DNA Probes
  • Female
  • Genetic Linkage
  • Humans
  • Lod Score
  • Male
  • Middle Aged
  • Pedigree
  • Polymorphism, Restriction Fragment Length
  • Sex Chromosome Aberrations / genetics*
  • Syndrome

Substances

  • DNA Probes