A polymorphism in intron 20 of the CFTR gene

Eitemau Tebyg

• A mutation in exon 7 of the CFTR gene is common in the western part of France.
  gan: Audrezet, M P, et al.
  Cyhoeddwyd: (1992)
• SSCP-polymorphism in intron 12 of the CFTR gene recognized by Bcll
  gan: Chillón, M., et al.
  Cyhoeddwyd: (1991)
• Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients.
  gan: Mercier, B, et al.
  Cyhoeddwyd: (1995)
• Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTR.
  gan: Lissens, W, et al.
  Cyhoeddwyd: (1993)
• G/A polymorphism in an intron of the fibrillin gene FBNI
  gan: Hewett, D.R., et al.
  Cyhoeddwyd: (1991)