Linkage relations of the locus for granular corneal dystrophy Groenouw type I with 35 polymorphic systems

Acta Ophthalmol (Copenh). 1989 Dec;67(6):721-3. doi: 10.1111/j.1755-3768.1989.tb04410.x.

Abstract

The paper presents preliminary results of linkage relations of the locus for granular corneal dystrophy Groenouw type I employing 35 classic genetic markers. Blood and saliva from 124 members of one family with this disorder were examined with the aim of localizing the disease to a certain chromosome. The highest lodscore was 1.04 in females at theta 0.00 to the system C1R, thus supplying a clue for continued gene-mapping investigations on the short arm of chromosome No. 12.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Child
  • Child, Preschool
  • Chromosomes, Human, Pair 12
  • Corneal Dystrophies, Hereditary / genetics*
  • Female
  • Genetic Linkage / genetics*
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Genetic / genetics*