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David Dimmock

Showing results (1-10 of 101) with videos related to

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Genome Medicine|June 28, 2012
A personal perspective on returning secondary results of clinical genome sequencingDavid Dimmock
Current Protocols in Human Genetics|April 19, 2013
Whole genome sequencing: a considered approach to clinical implementationDavid Dimmock
Current Opinion in Pediatrics|September 2, 2011
Whole exome and whole genome sequencingDavid Bick, David Dimmock
The New England Journal of Medicine|June 19, 2014
Clinical decisions. Screening an asymptomatic person for genetic riskWylie Burke, David Dimmock
Current Protocols in Human Genetics|January 15, 2011
Real-time quantitative PCR analysis of mitochondrial DNA contentVictor Venegas, Jing Wang, David Dimmock, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 18, 2011
Next-generation sequencing facilitates the diagnosis in a child with twinkle mutations causing cholestatic liver failureVi Goh, Daniel Helbling, Vincent Biank, et al.
The Journal of Pediatrics|August 14, 2021
Rapid whole-genome sequencing in critically Ill children: shifting from unease to evidence, education, and equitable implementationLinda S Franck, David Dimmock, Charlotte Hobbs, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 21, 2013
Reduced mitochondrial DNA content and heterozygous nuclear gene mutations in patients with acute liver failureDaniel Helbling, Adam Buchaklian, Jing Wang, et al.
Clinical Chemistry|May 8, 2010
Quantitative evaluation of the mitochondrial DNA depletion syndromeDavid Dimmock, Lin-Ya Tang, Eric S Schmitt, et al.
The Journal of Pediatrics|March 1, 2020
The Evaluation of Hematologic Screening and Perioperative Management in Patients with Noonan Syndrome: A Retrospective Chart ReviewBenjamin Briggs, Dipal Savla, Nanda Ramchandar, et al.
Pageof 11

Showing results (1-10 of 101) with videos related to

Sort By:
Pageof 11
Genome Medicine|June 28, 2012
A personal perspective on returning secondary results of clinical genome sequencingDavid Dimmock
Current Protocols in Human Genetics|April 19, 2013
Whole genome sequencing: a considered approach to clinical implementationDavid Dimmock
Current Opinion in Pediatrics|September 2, 2011
Whole exome and whole genome sequencingDavid Bick, David Dimmock
The New England Journal of Medicine|June 19, 2014
Clinical decisions. Screening an asymptomatic person for genetic riskWylie Burke, David Dimmock
Current Protocols in Human Genetics|January 15, 2011
Real-time quantitative PCR analysis of mitochondrial DNA contentVictor Venegas, Jing Wang, David Dimmock, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 18, 2011
Next-generation sequencing facilitates the diagnosis in a child with twinkle mutations causing cholestatic liver failureVi Goh, Daniel Helbling, Vincent Biank, et al.
The Journal of Pediatrics|August 14, 2021
Rapid whole-genome sequencing in critically Ill children: shifting from unease to evidence, education, and equitable implementationLinda S Franck, David Dimmock, Charlotte Hobbs, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 21, 2013
Reduced mitochondrial DNA content and heterozygous nuclear gene mutations in patients with acute liver failureDaniel Helbling, Adam Buchaklian, Jing Wang, et al.
Clinical Chemistry|May 8, 2010
Quantitative evaluation of the mitochondrial DNA depletion syndromeDavid Dimmock, Lin-Ya Tang, Eric S Schmitt, et al.
The Journal of Pediatrics|March 1, 2020
The Evaluation of Hematologic Screening and Perioperative Management in Patients with Noonan Syndrome: A Retrospective Chart ReviewBenjamin Briggs, Dipal Savla, Nanda Ramchandar, et al.
Pageof 11