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Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|July 30, 2014
[Genetics and epigenetics. Explanatory approaches for (gender-specific) mechanisms of disease development]K Zerres, T EggermannEuropean Journal of Human Genetics : EJHG|February 13, 2002
Evidence from skewed X inactivation for trisomy mosaicism in Silver-Russell syndromeA Sharp, G Moore, T EggermannClinical Nephrology|October 13, 2001
DNA diagnosis in hereditary nephropathiesK Zerres, T Eggermann, S Rudnik-SchönebornJournal of Inherited Metabolic Disease|January 26, 2006
Search for mutations in SLC1A5 (19q13) in cystinuria patientsE Brauers, U Vester, K Zerres, et al.Clinical Nephrology|April 25, 2006
Functional characterization of SLC7A9 polymorphisms assumed to influence the cystinuria phenotypeE Brauers, C Schmidt, K Zerres, et al.Der Internist|June 28, 2018
[Rational use of genetic tests in internal medicine : Possibilities and limitations of next generation sequencing diagnostics]M Elbracht, R Meyer, T Eggermann, et al.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Maternal uniparental disomy 16 and genetic counseling: new case and survey of published casesT Eggermann, M Curtis, K Zerres, et al.Annales De Genetique|January 9, 1999
A case of de novo translocation 16;21: trisomy 16q phenotype and origin of the aberrationT Eggermann, I Kolin-Gerresheim, F Gerresheim, et al.Annales De Genetique|January 1, 1993
Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counsellingT Eggermann, M M Nöthen, P Propping, et al.European Journal of Human Genetics : EJHG|November 28, 2000
Familial robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21U A Mau, U R Petruch, P Kaiser, et al.Pageof 7