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Birgit H Funke

Showing results (1-10 of 39) with videos related to

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Journal of Cardiovascular Translational Research|January 8, 2016
Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition GenesBirgit H Funke
Journal of Personalized Medicine|February 2, 2016
The Changing Landscape of Molecular Diagnostic Testing: Implications for Academic Medical CentersHeidi L Rehm, Elizabeth Hynes, Birgit H Funke
Current Protocols in Human Genetics|April 23, 2008
Selection of a platform for mutation detectionVictoria A Joshi, Debora Mancini-DiNardo, Birgit H Funke
Circulation. Arrhythmia and Electrophysiology|October 2, 2012
Dilated cardiomyopathyNeal K Lakdawala, Jeffery R Winterfield, Birgit H Funke
Human Mutation|April 27, 2018
NGS testing for cardiomyopathy: Utility of adding RASopathy-associated genesOzge Ceyhan-Birsoy, Maya M Miatkowski, Elizabeth Hynes, et al.
The Journal of Molecular Diagnostics : JMD|January 1, 2013
Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic eraPolakit Teekakirikul, Melissa A Kelly, Heidi L Rehm, et al.
Personalized Medicine|May 23, 2018
Platform evaluation for rapid genotyping of CYP2C9 and VKORC1 allelesVictoria A Joshi, Elizabeth Duffy, Birgit H Funke, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutationAudra L Bettinelli, Theodorus J Mulder, Birgit H Funke, et al.
The Journal of Molecular Diagnostics : JMD|September 19, 2016
Multiplexed Reference Materials as Controls for Diagnostic Next-Generation Sequencing: A Pilot Investigating Applications for Hypertrophic CardiomyopathyEmily M Kudalkar, Naif A M Almontashiri, Catherine Huang, et al.
BMJ Case Reports|January 25, 2013
NGS identifies TAZ mutation in a family with X-linked dilated cardiomyopathyElim Man, Katherine A Lafferty, Birgit H Funke, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Journal of Cardiovascular Translational Research|January 8, 2016
Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition GenesBirgit H Funke
Journal of Personalized Medicine|February 2, 2016
The Changing Landscape of Molecular Diagnostic Testing: Implications for Academic Medical CentersHeidi L Rehm, Elizabeth Hynes, Birgit H Funke
Current Protocols in Human Genetics|April 23, 2008
Selection of a platform for mutation detectionVictoria A Joshi, Debora Mancini-DiNardo, Birgit H Funke
Circulation. Arrhythmia and Electrophysiology|October 2, 2012
Dilated cardiomyopathyNeal K Lakdawala, Jeffery R Winterfield, Birgit H Funke
Human Mutation|April 27, 2018
NGS testing for cardiomyopathy: Utility of adding RASopathy-associated genesOzge Ceyhan-Birsoy, Maya M Miatkowski, Elizabeth Hynes, et al.
The Journal of Molecular Diagnostics : JMD|January 1, 2013
Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic eraPolakit Teekakirikul, Melissa A Kelly, Heidi L Rehm, et al.
Personalized Medicine|May 23, 2018
Platform evaluation for rapid genotyping of CYP2C9 and VKORC1 allelesVictoria A Joshi, Elizabeth Duffy, Birgit H Funke, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutationAudra L Bettinelli, Theodorus J Mulder, Birgit H Funke, et al.
The Journal of Molecular Diagnostics : JMD|September 19, 2016
Multiplexed Reference Materials as Controls for Diagnostic Next-Generation Sequencing: A Pilot Investigating Applications for Hypertrophic CardiomyopathyEmily M Kudalkar, Naif A M Almontashiri, Catherine Huang, et al.
BMJ Case Reports|January 25, 2013
NGS identifies TAZ mutation in a family with X-linked dilated cardiomyopathyElim Man, Katherine A Lafferty, Birgit H Funke, et al.
Pageof 4