DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysis

This publication has 15 references indexed in Scilit:

• Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia.
  Journal of Clinical Investigation, 1989
• A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene
  Genomics, 1988
• Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome
  American Journal of Medical Genetics, 1988
• Assignment of the locus order DXS28‐ DXS67‐DMD as a spin‐off from diagnostic DNA marker analysis in a family with Duchenne muscular dystrophy
  Clinical Genetics, 1987
• Long-range restriction map around the Duchenne muscular dystrophy gene
  Nature, 1986
• Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy
  Clinical Genetics, 1986
• Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families
  Human Genetics, 1985
• Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci
  Gene, 1985
• Report of the committee on the genetic constitution of the X and Y chromosomes
  Cytogenetic and Genome Research, 1985
• A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
  Analytical Biochemistry, 1984