Three RFLPs for pZ11 (DXS540) in the choroideremia gene at Xq21.2.

Benzer Materyaller

• Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis.
  Yazar:: van de Pol, T J, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21.
  Yazar:: Clark, P A, ve diğerleri
  Baskı/Yayın Bilgisi: (1994)
• Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.
  Yazar:: Merry, D E, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.
  Yazar:: Nussbaum, R L, ve diğerleri
  Baskı/Yayın Bilgisi: (1985)
• An anonymous single copy X-chromosome clone DXS92, from Xq26-27, identifies two frequent RFLPs.
  Yazar:: Davatelis, G, ve diğerleri
  Baskı/Yayın Bilgisi: (1985)