Linkage Between the X-linked Retinitis Pigmentosa Locus and the L1.28 Locus

This publication has 10 references indexed in Scilit:

• Detection of specific sequences among DNA fragments separated by gel electrophoresis
  Published by Elsevier ,2006
• MINOR XP21 CHROMOSOME DELETION IN A MALE ASSOCIATED WITH EXPRESSION OF DUCHENNE MUSCULAR-DYSTROPHY, CHRONIC GRANULOMATOUS-DISEASE, RETINITIS PIGMENTOSA, AND MCLEOD SYNDROME
  1985
• Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28
  Nature, 1984
• Prevalence of Retinitis Pigmentosa in Maine
  American Journal of Ophthalmology, 1984
• A STRATEGY TO REVEAL HIGH-FREQUENCY RFLPS ALONG THE HUMAN X-CHROMOSOME
  1984
• TOWARD A COMPLETE LINKAGE MAP OF THE HUMAN CHROMOSOME-X - REGIONAL ASSIGNMENT OF 16 CLONED SINGLE-COPY DNA-SEQUENCES EMPLOYING A PANEL OF SOMATIC-CELL HYBRIDS
  1984
• Extensions to Pedigree Analysis
  Human Heredity, 1982
• CONSTRUCTION OF A GENETIC-LINKAGE MAP IN MAN USING RESTRICTION FRAGMENT LENGTH POLYMORPHISMS
  1980
• Electroretinographic Testing as an Aid in Detection of Carriers of X-Chromosome-Linked Retinitis Pigmentosa
  American Journal of Ophthalmology, 1979
• Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.
  Proceedings of the National Academy of Sciences, 1977