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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: harms hk. Hum Genet. 1996 Jun;97(6):727-31. doi: 10.1007/BF02346181. Hum Genet. 1996. PMID: 8641688
Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.
Stanke F, Ballmann M, Bronsveld I, Dörk T, Gallati S, Laabs U, Derichs N, Ritzka M, Posselt HG, Harms HK, Griese M, Blau H, Mastella G, Bijman J, Veeze H, Tümmler B. Stanke F, et al. Among authors: harms hk. J Med Genet. 2008 Jan;45(1):47-54. doi: 10.1136/jmg.2007.053561. J Med Genet. 2008. PMID: 18178635 Free article.
[Diagnosis and therapy of cystic fibrosis-related diabetes].
Henke MO, Lang SM, Fischer R, Landgraf R, Huber RM, Bertele-Harms RM, Harms HK. Henke MO, et al. Among authors: harms hk. Pneumologie. 2004 Jan;58(1):36-9. doi: 10.1055/s-2003-812444. Pneumologie. 2004. PMID: 14732899 Review. German. No abstract available.
Renal function and renotropic effects of secretin in cystic fibrosis.
Windstetter D, Schaefer F, Schärer K, Reiter K, Eife R, Harms HK, Bertele-Harms R, Fiedler F, Tsui LC, Reitmeir P, Horster M, Hadorn HB. Windstetter D, et al. Among authors: harms hk. Eur J Med Res. 1997 Oct 30;2(10):431-6. Eur J Med Res. 1997. PMID: 9348270
35 results