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Lancet (London, England)|January 23, 1993
Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosisP Kubesch, T Dörk, U Wulbrand, et al.Journal of Medical Genetics|January 16, 1998
Novel and characteristic CFTR mutations in Saudi Arab children with severe cystic fibrosisE A el-Harith, T Dörk, M Stuhrmann, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|July 30, 1993
Cystic fibrosis: the impact of analytical technology for genotype-phenotype studiesB Tümmler, T Dörk, P Kubesch, et al.Pediatric Nephrology (Berlin, Germany)|May 11, 2000
Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuriaH Langen, D von Kietzell, D Byrd, et al.Human Mutation|January 1, 1996
Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markersN Morral, T Dörk, R Llevadot, et al.Gynecologic Oncology|March 4, 1999
Frequency of BRCA1 mutation 5382insC in German breast cancer patientsJ Backe, S Hofferbert, B Skawran, et al.Cancer Research|October 19, 2001
Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patientsT Dörk, R Bendix, M Bremer, et al.Journal of Ovarian Research|April 4, 2023
Targeted next-generation sequencing of 21 candidate genes in hereditary ovarian cancer patients from the Republic of BashkortostanD S Prokofyeva, E T Mingazheva, Ya V Valova, et al.Journal of Medical Genetics|January 8, 2008
Diversity of the basic defect of homozygous CFTR mutation genotypes in humansF Stanke, M Ballmann, I Bronsveld, et al.Human Genetics|September 1, 1997
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferensT Dörk, B Dworniczak, C Aulehla-Scholz, et al.Pageof 6