Dörk T - Search Results

1

Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens.

Dörk T, Dworniczak B, Aulehla-Scholz C, Wieczorek D, Böhm I, Mayerova A, Seydewitz HH, Nieschlag E, Meschede D, Horst J, Pander HJ, Sperling H, Ratjen F, Passarge E, Schmidtke J, Stuhrmann M. Dörk T, et al. Hum Genet. 1997 Sep;100(3-4):365-77. doi: 10.1007/s004390050518. Hum Genet. 1997. PMID: 9272157

2

A termination mutation (2143delT) in the CFTR gene of German cystic fibrosis patients.

Dörk T, Kälin N, Stuhrmann M, Schmidtke J, Tümmler B. Dörk T, et al. Hum Genet. 1992 Nov;90(3):279-84. doi: 10.1007/BF00220079. Hum Genet. 1992. PMID: 1283149

3

Distribution patterns of the delta F508 mutation in the CFTR gene of CF-linked marker haplotypes in the German population.

Reis A, Bremer S, Schlösser M, Dueck M, Böhm I, Hundrieser J, Macek M, Stuhrmann M, Wagner M, Dörk T, et al. Reis A, et al. Among authors: dork t. Hum Genet. 1990 Sep;85(4):421-2. doi: 10.1007/BF02428292. Hum Genet. 1990. PMID: 2210758

4

Transcript analysis of CFTR nonsense mutations in lymphocytes and nasal epithelial cells from cystic fibrosis patients.

Will K, Dörk T, Stuhrmann M, von der Hardt H, Ellemunter H, Tümmler B, Schmidtke J. Will K, et al. Among authors: dork t. Hum Mutat. 1995;5(3):210-20. doi: 10.1002/humu.1380050305. Hum Mutat. 1995. PMID: 7541274

5

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: dork t. Hum Genet. 1996 Jun;97(6):727-31. doi: 10.1007/BF02346181. Hum Genet. 1996. PMID: 8641688

6

Detection of 100% of the CFTR mutations in 63 CF families from Tyrol.

Stuhrmann M, Dörk T, Frühwirth M, Golla A, Skawran B, Antonin W, Ebhardt M, Loos A, Ellemunter H, Schmidtke J. Stuhrmann M, et al. Among authors: dork t. Clin Genet. 1997 Oct;52(4):240-6. doi: 10.1111/j.1399-0004.1997.tb02555.x. Clin Genet. 1997. PMID: 9383031

7

Novel and characteristic CFTR mutations in Saudi Arab children with severe cystic fibrosis.

el-Harith EA, Dörk T, Stuhrmann M, Abu-Srair H, al-Shahri A, Keller KM, Lentze MJ, Schmidtke J. el-Harith EA, et al. Among authors: dork t. J Med Genet. 1997 Dec;34(12):996-9. doi: 10.1136/jmg.34.12.996. J Med Genet. 1997. PMID: 9429141 Free PMC article.

8

CFTR gene mutations and male infertility.

Stuhrmann M, Dörk T. Stuhrmann M, et al. Among authors: dork t. Andrologia. 2000 Mar;32(2):71-83. doi: 10.1046/j.1439-0272.2000.00327.x. Andrologia. 2000. PMID: 10755189 Review.

9

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.

Dörk T, Macek M Jr, Mekus F, Tümmler B, Tzountzouris J, Casals T, Krebsová A, Koudová M, Sakmaryová I, Macek M Sr, Vávrová V, Zemková D, Ginter E, Petrova NV, Ivaschenko T, Baranov V, Witt M, Pogorzelski A, Bal J, Zékanowsky C, Wagner K, Stuhrmann M, Bauer I, Seydewitz HH, Neumann T, Jakubiczka S. Dörk T, et al. Hum Genet. 2000 Mar;106(3):259-68. doi: 10.1007/s004390000246. Hum Genet. 2000. PMID: 10798353

10

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.

Dörk T, Neumann T, Wulbrand U, Wulf B, Kälin N, Maass G, Krawczak M, Guillermit H, Ferec C, Horn G, et al. Dörk T, et al. Hum Genet. 1992 Feb;88(4):417-25. doi: 10.1007/BF00215676. Hum Genet. 1992. PMID: 1371263

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

399 results

Search Page

Filters