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Marc S Greenblatt

Showing results (1-10 of 53) with videos related to

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Human Mutation|February 18, 2010
Mutation clusters offer insight into predicting pathogenicityMarc S Greenblatt
Surgical Oncology Clinics of North America|September 14, 2015
Sequence Variants of Uncertain Significance: What to Do When Genetic Test Results Are Not DefinitiveMarc S Greenblatt
Familial Cancer|March 26, 2013
Gene variants of unknown clinical significance in Lynch syndrome. An introduction for cliniciansRolf H Sijmons, Marc S Greenblatt, Maurizio Genuardi
Human Mutation|October 28, 2008
In silico analysis of missense substitutions using sequence-alignment based methodsSean V Tavtigian, Marc S Greenblatt, Fabienne Lesueur, et al.
Human Mutation|October 28, 2008
Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working GroupSean V Tavtigian, Marc S Greenblatt, David E Goldgar, et al.
Familial Cancer|April 30, 2017
Placing negative multi-gene panel results into clinical contextDavid J Hermel, Wendy C McKinnon, Marie E Wood, et al.
Familial Cancer|July 13, 2016
Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer ProgramDavid J Hermel, Wendy C McKinnon, Marie E Wood, et al.
Human Mutation|January 29, 2014
Clinically relevant variants - identifying, collecting, interpreting, and disseminating: the 2013 annual scientific meeting of the Human Genome Variation SocietyChristine M Stanley, Shamil R Sunyaev, Marc S Greenblatt, et al.
Human Mutation|September 15, 2004
The CDKN2A database: Integrating allelic variants with evolution, structure, function, and disease associationJoan A Murphy, Ramiro Barrantes-Reynolds, Rama Kocherlakota, et al.
Human Mutation|January 20, 2015
Germline & somatic mosaicism: the 2014 annual scientific meeting of the Human Genome Variation SocietyWilliam S Oetting, Marc S Greenblatt, Anthony J Brookes, et al.
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
Human Mutation|February 18, 2010
Mutation clusters offer insight into predicting pathogenicityMarc S Greenblatt
Surgical Oncology Clinics of North America|September 14, 2015
Sequence Variants of Uncertain Significance: What to Do When Genetic Test Results Are Not DefinitiveMarc S Greenblatt
Familial Cancer|March 26, 2013
Gene variants of unknown clinical significance in Lynch syndrome. An introduction for cliniciansRolf H Sijmons, Marc S Greenblatt, Maurizio Genuardi
Human Mutation|October 28, 2008
In silico analysis of missense substitutions using sequence-alignment based methodsSean V Tavtigian, Marc S Greenblatt, Fabienne Lesueur, et al.
Human Mutation|October 28, 2008
Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working GroupSean V Tavtigian, Marc S Greenblatt, David E Goldgar, et al.
Familial Cancer|April 30, 2017
Placing negative multi-gene panel results into clinical contextDavid J Hermel, Wendy C McKinnon, Marie E Wood, et al.
Familial Cancer|July 13, 2016
Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer ProgramDavid J Hermel, Wendy C McKinnon, Marie E Wood, et al.
Human Mutation|January 29, 2014
Clinically relevant variants - identifying, collecting, interpreting, and disseminating: the 2013 annual scientific meeting of the Human Genome Variation SocietyChristine M Stanley, Shamil R Sunyaev, Marc S Greenblatt, et al.
Human Mutation|September 15, 2004
The CDKN2A database: Integrating allelic variants with evolution, structure, function, and disease associationJoan A Murphy, Ramiro Barrantes-Reynolds, Rama Kocherlakota, et al.
Human Mutation|January 20, 2015
Germline & somatic mosaicism: the 2014 annual scientific meeting of the Human Genome Variation SocietyWilliam S Oetting, Marc S Greenblatt, Anthony J Brookes, et al.
Pageof 6