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Elke Holinski-Feder

Showing results (1-10 of 174) with videos related to

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MMW Fortschritte Der Medizin|April 17, 2019
[Colorectal cancer prevention and early detection: what is the best strategy?]Manfred Gross, Elke Holinski-Feder
Pathologie (Heidelberg, Germany)|June 12, 2024
[Lynch syndrome]Verena Steinke-Lange, Elke Holinski-Feder
Visceral Medicine|October 12, 2019
Genetic Screening and Personalized Prevention in Colorectal CancerVerena Steinke-Lange, Elke Holinski-Feder
MMW Fortschritte Der Medizin|June 4, 2021
[Hereditary non-polyposis tumor risk syndromes]Verena Steinke-Lange, Elke Holinski-Feder
Cardiology|January 29, 2011
Recovery of systolic dysfunction in duchenne muscular dystrophy due to the point mutation c.4213C>TJosef Finsterer, Claudia Stöllberger, Elke Holinski-Feder
Clinical Laboratory|August 12, 2003
Easy, accurate and reliable screening for SNPs by ion pair/reverse phase HPLC: simultaneous detection of factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase C677T variantsBirgit Neitzel, Christine Matern, Elke Holinski-Feder
Cancer Genetics and Cytogenetics|May 15, 2007
A new interphase fluorescence in situ hybridization approach for genomic rearrangements involving MLH1 and MSH6 in hereditary nonpolyposis colorectal cancer-suspected mutation-negative patientsUdo Koehler, Monika Grabowski, Ulrike Bacher, et al.
International Journal of Molecular Sciences|October 29, 2025
Next-Generation Sequencing in Congenital Eye Malformations: Identification of Genetic Causes and Comparison of Different Panel-Based Diagnostic StrategiesLukas Neuhann, Andreas Laner, Elke Holinski-Feder, et al.
European Journal of Cancer (Oxford, England : 1990)|January 4, 2011
First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genesMonika Morak, Trisari Massdorf, Helena Sykora, et al.
European Journal of Gastroenterology & Hepatology|December 3, 2008
Report on de-novo mutation in the MSH2 gene as a rare event in hereditary nonpolyposis colorectal cancerMonika Morak, Andreas Laner, Michael Scholz, et al.
Pageof 18

Showing results (1-10 of 174) with videos related to

Sort By:
Pageof 18
MMW Fortschritte Der Medizin|April 17, 2019
[Colorectal cancer prevention and early detection: what is the best strategy?]Manfred Gross, Elke Holinski-Feder
Pathologie (Heidelberg, Germany)|June 12, 2024
[Lynch syndrome]Verena Steinke-Lange, Elke Holinski-Feder
Visceral Medicine|October 12, 2019
Genetic Screening and Personalized Prevention in Colorectal CancerVerena Steinke-Lange, Elke Holinski-Feder
MMW Fortschritte Der Medizin|June 4, 2021
[Hereditary non-polyposis tumor risk syndromes]Verena Steinke-Lange, Elke Holinski-Feder
Cardiology|January 29, 2011
Recovery of systolic dysfunction in duchenne muscular dystrophy due to the point mutation c.4213C>TJosef Finsterer, Claudia Stöllberger, Elke Holinski-Feder
Clinical Laboratory|August 12, 2003
Easy, accurate and reliable screening for SNPs by ion pair/reverse phase HPLC: simultaneous detection of factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase C677T variantsBirgit Neitzel, Christine Matern, Elke Holinski-Feder
Cancer Genetics and Cytogenetics|May 15, 2007
A new interphase fluorescence in situ hybridization approach for genomic rearrangements involving MLH1 and MSH6 in hereditary nonpolyposis colorectal cancer-suspected mutation-negative patientsUdo Koehler, Monika Grabowski, Ulrike Bacher, et al.
International Journal of Molecular Sciences|October 29, 2025
Next-Generation Sequencing in Congenital Eye Malformations: Identification of Genetic Causes and Comparison of Different Panel-Based Diagnostic StrategiesLukas Neuhann, Andreas Laner, Elke Holinski-Feder, et al.
European Journal of Cancer (Oxford, England : 1990)|January 4, 2011
First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genesMonika Morak, Trisari Massdorf, Helena Sykora, et al.
European Journal of Gastroenterology & Hepatology|December 3, 2008
Report on de-novo mutation in the MSH2 gene as a rare event in hereditary nonpolyposis colorectal cancerMonika Morak, Andreas Laner, Michael Scholz, et al.
Pageof 18