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CFTR protein analysis of splice site mutation 2789+5 G-A.
van Barneveld A, Stanke F, Claass A, Ballmann M, Tümmler B. van Barneveld A, et al. Among authors: claass a. J Cyst Fibros. 2008 Mar;7(2):165-7. doi: 10.1016/j.jcf.2007.07.007. Epub 2007 Aug 16. J Cyst Fibros. 2008. PMID: 17707141 Free article.
Geographic distribution and origin of CFTR mutations in Germany.
Tümmler B, Storrs T, Dziadek V, Dörk T, Meitinger T, Golla A, Bertele-Harms RM, Harms HK, Schröder E, Claass A, Rutjes J, Schneppenheim R, Bauer I, Breuel K, Stuhrmann M, Schmidtke J, Lindner M, Eigel A, Horst J, Kaiser R, Lentze MJ, Schmidt K, von der Hardt H, Estivill X. Tümmler B, et al. Among authors: claass a. Hum Genet. 1996 Jun;97(6):727-31. doi: 10.1007/BF02346181. Hum Genet. 1996. PMID: 8641688
The nasal polyps as a tool for basic research in cystic fibrosis.
Bautsch W, Ponelies N, Darnedde T, Fryburg K, Grothues D, Hundrieser J, Miller K, Monajembashi S, Claass A, Greulich KO, et al. Bautsch W, et al. Among authors: claass a. Scand J Gastroenterol Suppl. 1988;143:5-8. doi: 10.3109/00365528809090206. Scand J Gastroenterol Suppl. 1988. PMID: 2455330
Long term culture of nasal epithelial cells.
Claass A, Claus S, Höft J, Prange E. Claass A, et al. Acta Histochem. 1991;90(1):21-6. doi: 10.1016/S0065-1281(11)80152-2. Acta Histochem. 1991. PMID: 2048386
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