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Molecular Human Reproduction|May 12, 2010
Lymphatic capillary hypoplasia in the skin of fetuses with increased nuchal translucency and Turner's syndrome: comparison with trisomies and controlsC S von Kaisenberg, J Wilting, T Dörk, et al.Neuropediatrics|September 13, 2006
Interleukin-10 high producer allele and ultrasound-defined periventricular white matter abnormalities in preterm infants: a preliminary studyM Dördelmann, J Kerk, F Dressler, et al.Human Genetics|November 1, 1994
Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patientsT Dörk, F Mekus, K Schmidt, et al.Human Genetics|February 1, 1992
Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis familiesT Dörk, T Neumann, U Wulbrand, et al.Human Genetics|August 11, 1992
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) geneL Osborne, G Santis, M Schwarz, et al.Voprosy Onkologii|April 18, 2008
[Frequency of 5382insC mutation of the BRCA1 gene]M A Bermisheva, G F Zinnamullina, Sh Kh Gantsev, et al.Clinical Genetics|January 24, 1998
Detection of 100% of the CFTR mutations in 63 CF families from TyrolM Stuhrmann, T Dörk, M Frühwirth, et al.Genetika|January 26, 2018
[The search for new candidate genes involved in ovarian cancer pathogenesis by exome sequencing]D S Prokofyeva, E T Mingajeva, N V Bogdanova, et al.Human Genetics|September 1, 1990
Distribution patterns of the delta F508 mutation in the CFTR gene of CF-linked marker haplotypes in the German populationA Reis, S Bremer, M Schlösser, et al.Advances in Experimental Medicine and Biology|January 1, 1991
Genotype-phenotype correlations in cystic fibrosis patientsM Stuhrmann, T Dörk, M Krawczak, et al.Pageof 6