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Characterization of ATM gene mutations in 66 ataxia telangiectasia families.
Sandoval N, Platzer M, Rosenthal A, Dörk T, Bendix R, Skawran B, Stuhrmann M, Wegner RD, Sperling K, Banin S, Shiloh Y, Baumer A, Bernthaler U, Sennefelder H, Brohm M, Weber BH, Schindler D. Sandoval N, et al. Among authors: skawran b. Hum Mol Genet. 1999 Jan;8(1):69-79. doi: 10.1093/hmg/8.1.69. Hum Mol Genet. 1999. PMID: 9887333
Frequency of BRCA1 mutation 5382insC in German breast cancer patients.
Backe J, Hofferbert S, Skawran B, Dörk T, Stuhrmann M, Karstens JH, Untch M, Meindl A, Burgemeister R, Chang-Claude J, Weber BH. Backe J, et al. Among authors: skawran b. Gynecol Oncol. 1999 Mar;72(3):402-6. doi: 10.1006/gyno.1998.5270. Gynecol Oncol. 1999. PMID: 10053113
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: skawran b. Clin Genet. 1997 Oct;52(4):240-6. doi: 10.1111/j.1399-0004.1997.tb02555.x. Clin Genet. 1997. PMID: 9383031
Characterization of a human TSPY promoter.
Skawran B, Schubert S, Dechend F, Vervoorts J, Nayernia K, Lüscher B, Schmidtke J. Skawran B, et al. Mol Cell Biochem. 2005 Aug;276(1-2):159-67. doi: 10.1007/s11010-005-3801-x. Mol Cell Biochem. 2005. PMID: 16132697
45 results