Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q.

Samankaltaisia teoksia

• A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1
  Tekijä: Michaelides, M, et al.
  Julkaistu: (2005)
• Refinement of the cone-rod retinal dystrophy locus on chromosome 19q.
  Tekijä: Gregory, C. Y., et al.
  Julkaistu: (1994)
• A retGC-1 mutation in autosomal dominant cone-rod dystrophy.
  Tekijä: Perrault, I, et al.
  Julkaistu: (1998)
• A detailed phenotypic study of “cone dystrophy with supernormal rod ERG”
  Tekijä: Michaelides, M, et al.
  Julkaistu: (2005)
• Meiotic drive at the myotonic dystrophy and the cone-rod dystrophy loci on chromosome 19q13.3.
  Tekijä: Inglehearn, C F, et al.
  Julkaistu: (1997)