Author:
Burggraf Siegfried,Malik Naeem,Schuhmacher Edith,Olgemöller Bernhard
Publisher
Springer Berlin Heidelberg
Reference8 articles.
1. Farber S (1945) Some organic digestive disturbances in early life. Pathological changes associated with pancreatic insufficiency. Mich Med Soc 44: 587–594
2. Widdicombe JH, Welsh MJ, Finkbeiner WE (1985) Cystic fibrosis decreases the apical membrane chloride permeability of monolayers cultured from cells of tracheal epithelium. Proc Natl Acad Sci USA 82: 6167–6171
3. Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, Chakravarti A, Buchwald M, Tsui LC (1989) Identification of the cystic fibrosis gene: genetic analysis. Science 245: 1073–1080
4. Deufel T, Rabe H, Wieser T, Meitinger T, Rosenecker J, Bertele-Harms R, Harms K, Hadorn HB, Roscher AA (1993) Mutation analysis in the diagnosis of cystic fibrosis. Eur J Pediatr 152: 909–911
5. Tümmler B, Storrs T, Dziadek V. et al. (1996) Geographic distribution and origin of CFTR mutations in Germany. Hum Genet 97: 727–731