Deletions in the 5' region of dystrophin and resulting phenotypes.

Benzer Materyaller

• Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene.
  Yazar:: Abbs, S, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)
• Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.
  Yazar:: Sherratt, T G, ve diğerleri
  Baskı/Yayın Bilgisi: (1993)
• Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion
  Yazar:: Gualandi, F, ve diğerleri
  Baskı/Yayın Bilgisi: (2003)
• A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart.
  Yazar:: Muntoni, F, ve diğerleri
  Baskı/Yayın Bilgisi: (1995)
• A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.
  Yazar:: Abbs, S, ve diğerleri
  Baskı/Yayın Bilgisi: (1991)