Laws regarding insurance companies.

This publication has 12 references indexed in Scilit:

• Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene (CRX) Essential for Maintenance of the Photoreceptor
  Published by Elsevier ,1997
• Analysis of the RPGRGene in 11 Pedigrees with the Retinitis Pigmentosa Type 3 Genotype: Paucity of Mutations in the Coding Region but Splice Defects in Two Families
  American Journal of Human Genetics, 1997
• Genetic and Physical Localisation of the Gene Causing Cone-Rod Dystrophy (CORD2)
  Published by Springer Nature ,1997
• Handbook of Human Genetic Linkage.
  Published by JSTOR ,1996
• A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3)
  Nature Genetics, 1996
• A comprehensive genetic map of the human genome based on 5,264 microsatellites
  Nature, 1996
• Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypes.
  Genome Research, 1996
• Chromosome 19q Cone-Rod Retinal Dystrophy
  Archives of Ophthalmology (1950), 1995
• Genetic linkage of cone–rod retinal dystrophy to chromosome 19q and evidence for segregation distortion
  Nature Genetics, 1994
• Yeast artificial chromosome libraries containing large inserts from mouse and human DNA.
  Proceedings of the National Academy of Sciences, 1991