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David P Dimmock

Showing results (1-10 of 38) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2016
Should states adopt newborn screening for early infantile Krabbe disease?David P Dimmock
Pediatric Clinics of North America|November 30, 2016
Presentation and Diagnostic Evaluation of Mitochondrial DiseaseDavid P Dimmock, Michael W Lawlor
Clinics in Perinatology|December 3, 2014
Ethical issues in DNA sequencing in the neonateDavid P Dimmock, David P Bick
Human Mutation|June 20, 2022
Better and faster is cheaperErica F Sanford Kobayashi, David P Dimmock
Molecular Genetics and Metabolism|May 25, 2012
Recessive deoxyguanosine kinase deficiency causes juvenile onset mitochondrial myopathyAdam H Buchaklian, Daniel Helbling, Stephanie M Ware, et al.
Pediatric Cardiology|September 4, 2014
Hypertrophic cardiomyopathy: a new mutation illustrates the need for family-centered careDaniel D Lee, Regan L Veith, David P Dimmock, et al.
Pediatrics|May 13, 2015
SIGIRR genetic variants in premature infants with necrotizing enterocolitisVenkatesh Sampath, Heather Menden, Daniel Helbling, et al.
Human Gene Therapy|August 22, 2022
Immune Responses and Immunosuppressive Strategies for Adeno-Associated Virus-Based Gene Therapy for Treatment of Central Nervous System Disorders: Current Knowledge and ApproachesSuyash Prasad, David P Dimmock, Benjamin Greenberg, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 22, 2020
An online compendium of treatable genetic disordersDavid Bick, Sarah L Bick, David P Dimmock, et al.
Frontiers in Pediatrics|March 31, 2023
Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary systemErika T Allred, Elliot A Perens, Nicole G Coufal, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2016
Should states adopt newborn screening for early infantile Krabbe disease?David P Dimmock
Pediatric Clinics of North America|November 30, 2016
Presentation and Diagnostic Evaluation of Mitochondrial DiseaseDavid P Dimmock, Michael W Lawlor
Clinics in Perinatology|December 3, 2014
Ethical issues in DNA sequencing in the neonateDavid P Dimmock, David P Bick
Human Mutation|June 20, 2022
Better and faster is cheaperErica F Sanford Kobayashi, David P Dimmock
Molecular Genetics and Metabolism|May 25, 2012
Recessive deoxyguanosine kinase deficiency causes juvenile onset mitochondrial myopathyAdam H Buchaklian, Daniel Helbling, Stephanie M Ware, et al.
Pediatric Cardiology|September 4, 2014
Hypertrophic cardiomyopathy: a new mutation illustrates the need for family-centered careDaniel D Lee, Regan L Veith, David P Dimmock, et al.
Pediatrics|May 13, 2015
SIGIRR genetic variants in premature infants with necrotizing enterocolitisVenkatesh Sampath, Heather Menden, Daniel Helbling, et al.
Human Gene Therapy|August 22, 2022
Immune Responses and Immunosuppressive Strategies for Adeno-Associated Virus-Based Gene Therapy for Treatment of Central Nervous System Disorders: Current Knowledge and ApproachesSuyash Prasad, David P Dimmock, Benjamin Greenberg, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 22, 2020
An online compendium of treatable genetic disordersDavid Bick, Sarah L Bick, David P Dimmock, et al.
Frontiers in Pediatrics|March 31, 2023
Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary systemErika T Allred, Elliot A Perens, Nicole G Coufal, et al.
Pageof 4