Localization of the Gene for Autosomal Recessive Congenital Hereditary Endothelial Dystrophy (CHED2) to Chromosome 20 by Homozygosity Mapping

This publication has 15 references indexed in Scilit:

• Fast and sensitive silver staining of DNA in polyacrylamide gels
  Published by Elsevier ,2004
• Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct
  British Journal of Ophthalmology, 1999
• A comprehensive genetic map of the human genome based on 5,264 microsatellites
  Nature, 1996
• The 1993–94 Généthon human genetic linkage map
  Nature Genetics, 1994
• Homozygosity Mapping: A Way to Map Human Recessive Traits with the DNA of Inbred Children
  Science, 1987
• Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis
  Genetic Epidemiology, 1986
• Strategies for multilocus linkage analysis in humans.
  Proceedings of the National Academy of Sciences, 1984
• Similarities between Posterior Polymorphous and Congenital Hereditary Endothelial Dystrophies
  Cornea, 1982
• The Clinical Spectrum of Posterior Polymorphous Dystrophy
  Archives of Ophthalmology (1950), 1977
• Congenital Hereditary Corneal Dystrophy*
  American Journal of Ophthalmology, 1960