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David N Cooper

Showing results (61-70 of 398) with videos related to

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Genes|October 23, 2021
Atypical <i>NF1</i> Microdeletions: Challenges and Opportunities for Genotype/Phenotype Correlations in Patients with Large <i>NF1</i> DeletionsHildegard Kehrer-Sawatzki, Ute Wahlländer, David N Cooper, et al.
Plos One|July 11, 2015
Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological SenseSabine Siegert, Andreas Wolf, David N Cooper, et al.
Forensic Science International. Genetics|December 20, 2011
How to distinguish genetically between an alleged father and his monozygotic twin: a thought experimentMichael Krawczak, David N Cooper, Fred Fändrich, et al.
Human Mutation|February 20, 2004
Gross Rearrangement Breakpoint Database (GRaBD)Shaun S Abeysinghe, Peter D Stenson, Michael Krawczak, et al.
Human Genetics|December 7, 2016
The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesisHildegard Kehrer-Sawatzki, Said Farschtschi, Victor-Felix Mautner, et al.
Nucleic Acids Research|April 17, 2016
Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequencesAlbino Bacolla, John A Tainer, Karen M Vasquez, et al.
Genetics Research International|April 18, 2015
Genetics in genomic eraEugenia Poliakov, David N Cooper, Elena I Stepchenkova, et al.
Human Genomics|December 14, 2011
Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesisSebastian Laycock-van Spyk, Nick Thomas, David N Cooper, et al.
Human Genomics|July 24, 2010
Characterisation of a functional intronic polymorphism in the human growth hormone (GH1) geneDavid S Millar, Martin Horan, Nadia A Chuzhanova, et al.
Human Genomics|December 19, 2012
Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?Adila Alkindy, Nadia Chuzhanova, Usha Kini, et al.
Pageof 40

Showing results (61-70 of 398) with videos related to

Sort By:
Pageof 40
Genes|October 23, 2021
Atypical <i>NF1</i> Microdeletions: Challenges and Opportunities for Genotype/Phenotype Correlations in Patients with Large <i>NF1</i> DeletionsHildegard Kehrer-Sawatzki, Ute Wahlländer, David N Cooper, et al.
Plos One|July 11, 2015
Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological SenseSabine Siegert, Andreas Wolf, David N Cooper, et al.
Forensic Science International. Genetics|December 20, 2011
How to distinguish genetically between an alleged father and his monozygotic twin: a thought experimentMichael Krawczak, David N Cooper, Fred Fändrich, et al.
Human Mutation|February 20, 2004
Gross Rearrangement Breakpoint Database (GRaBD)Shaun S Abeysinghe, Peter D Stenson, Michael Krawczak, et al.
Human Genetics|December 7, 2016
The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesisHildegard Kehrer-Sawatzki, Said Farschtschi, Victor-Felix Mautner, et al.
Nucleic Acids Research|April 17, 2016
Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequencesAlbino Bacolla, John A Tainer, Karen M Vasquez, et al.
Genetics Research International|April 18, 2015
Genetics in genomic eraEugenia Poliakov, David N Cooper, Elena I Stepchenkova, et al.
Human Genomics|December 14, 2011
Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesisSebastian Laycock-van Spyk, Nick Thomas, David N Cooper, et al.
Human Genomics|July 24, 2010
Characterisation of a functional intronic polymorphism in the human growth hormone (GH1) geneDavid S Millar, Martin Horan, Nadia A Chuzhanova, et al.
Human Genomics|December 19, 2012
Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?Adila Alkindy, Nadia Chuzhanova, Usha Kini, et al.
Pageof 40