Linkage studies and deletion screening in choroideremia.

Lignende værker

• Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.
  af: Lesko, J G, et al.
  Udgivet: (1987)
• Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.
  af: Merry, D E, et al.
  Udgivet: (1989)
• Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation.
  af: Nussbaum, R L, et al.
  Udgivet: (1987)
• Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases
  af: Cremers, Frans P. M., et al.
  Udgivet: (1990)
• Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.
  af: Nussbaum, R L, et al.
  Udgivet: (1985)