Linkage studies and deletion screening in choroideremia.

類似資料

• Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.
  著者:: Lesko, J G, 等
  出版事項: (1987)
• Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.
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• Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation.
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  出版事項: (1987)
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• Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.
  著者:: Nussbaum, R L, 等
  出版事項: (1985)