Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation.

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)
• Linkage studies and deletion screening in choroideremia.
  af: Wright, A F, et al.
  Udgivet: (1990)
• Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres
  af: Slavotinek, A, et al.
  Udgivet: (1999)
• A maternally inherited 8.05 Mb Xq21 deletion associated with Choroideremia, deafness, and mental retardation syndrome in a male patient
  af: Liang, Siying, et al.
  Udgivet: (2017)