Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David N Cooper

Showing results (1-10 of 398) with videos related to

Pageof 40
Sort By:
Human Genomics|July 24, 2010
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genesDavid N Cooper
Human Genetics|May 27, 2011
Lionizing lyonization 50 years onDavid N Cooper
Expert Review of Molecular Diagnostics|April 19, 2002
Molecular diagnosis of facioscapulohumeral muscular dystrophyMeena Upadhyaya, David N Cooper
Genetic Testing and Molecular Biomarkers|April 7, 2010
Do inherited disease genes have distinguishing functional characteristics?David N Cooper, Matthew Mort
Human Genomics|November 26, 2010
Prospects for the automated extraction of mutation data from the scientific literaturePeter D Stenson, David N Cooper
Human Genetics|September 18, 2021
Classification of NF1 microdeletions and its importance for establishing genotype/phenotype correlations in patients with NF1 microdeletionsHildegard Kehrer-Sawatzki, David N Cooper
Human Genetics|December 20, 2021
Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variantsHildegard Kehrer-Sawatzki, David N Cooper
Human Genetics|November 29, 2014
A changing of the guard at human geneticsDavid N Cooper, Cynthia C Morton
Human Mutation|March 8, 2016
A Mechanistic Link between L1 Retrotransposition and ChromothripsisJian-Min Chen, David N Cooper
European Journal of Human Genetics : EJHG|March 18, 2010
GWAS: heritability missing in action?Angus J Clarke, David N Cooper
Pageof 40

Showing results (1-10 of 398) with videos related to

Sort By:
Pageof 40
Human Genomics|July 24, 2010
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genesDavid N Cooper
Human Genetics|May 27, 2011
Lionizing lyonization 50 years onDavid N Cooper
Expert Review of Molecular Diagnostics|April 19, 2002
Molecular diagnosis of facioscapulohumeral muscular dystrophyMeena Upadhyaya, David N Cooper
Genetic Testing and Molecular Biomarkers|April 7, 2010
Do inherited disease genes have distinguishing functional characteristics?David N Cooper, Matthew Mort
Human Genomics|November 26, 2010
Prospects for the automated extraction of mutation data from the scientific literaturePeter D Stenson, David N Cooper
Human Genetics|September 18, 2021
Classification of NF1 microdeletions and its importance for establishing genotype/phenotype correlations in patients with NF1 microdeletionsHildegard Kehrer-Sawatzki, David N Cooper
Human Genetics|December 20, 2021
Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variantsHildegard Kehrer-Sawatzki, David N Cooper
Human Genetics|November 29, 2014
A changing of the guard at human geneticsDavid N Cooper, Cynthia C Morton
Human Mutation|March 8, 2016
A Mechanistic Link between L1 Retrotransposition and ChromothripsisJian-Min Chen, David N Cooper
European Journal of Human Genetics : EJHG|March 18, 2010
GWAS: heritability missing in action?Angus J Clarke, David N Cooper
Pageof 40