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David Dimmock

Showing results (51-60 of 101) with videos related to

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NPJ Genomic Medicine|May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine|April 23, 2021
Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
BMC Health Services Research|November 8, 2020
At the intersection of precision medicine and population health: an implementation-effectiveness study of family health history based systematic risk assessment in primary careLori A Orlando, R Ryanne Wu, Rachel A Myers, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
NPJ Genomic Medicine|February 26, 2024
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disordersKristen M Wigby, Deanna Brockman, Gregory Costain, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
BMC Health Services Research|December 6, 2022
Implementation-effectiveness trial of systematic family health history based risk assessment and impact on clinical disease prevention and surveillance activitiesR Ryanne Wu, Rachel A Myers, Joan Neuner, et al.
Oncogene|August 30, 2019
The mitochondrial carrier Citrin plays a role in regulating cellular energy during carcinogenesisShiran Rabinovich, Alon Silberman, Lital Adler, et al.
Orphanet Journal of Rare Diseases|July 20, 2023
Correction to: The evolution of the mitochondrial disease diagnostic odysseyJohn L P Thompson, Amel Karaa, Hung Pham, et al.
Orphanet Journal of Rare Diseases|June 22, 2023
The evolution of the mitochondrial disease diagnostic odysseyJohn L P Thompson, Amel Karaa, Hung Pham, et al.
Pageof 11

Showing results (51-60 of 101) with videos related to

Sort By:
Pageof 11
NPJ Genomic Medicine|May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine|April 23, 2021
Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
BMC Health Services Research|November 8, 2020
At the intersection of precision medicine and population health: an implementation-effectiveness study of family health history based systematic risk assessment in primary careLori A Orlando, R Ryanne Wu, Rachel A Myers, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
NPJ Genomic Medicine|February 26, 2024
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disordersKristen M Wigby, Deanna Brockman, Gregory Costain, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
BMC Health Services Research|December 6, 2022
Implementation-effectiveness trial of systematic family health history based risk assessment and impact on clinical disease prevention and surveillance activitiesR Ryanne Wu, Rachel A Myers, Joan Neuner, et al.
Oncogene|August 30, 2019
The mitochondrial carrier Citrin plays a role in regulating cellular energy during carcinogenesisShiran Rabinovich, Alon Silberman, Lital Adler, et al.
Orphanet Journal of Rare Diseases|July 20, 2023
Correction to: The evolution of the mitochondrial disease diagnostic odysseyJohn L P Thompson, Amel Karaa, Hung Pham, et al.
Orphanet Journal of Rare Diseases|June 22, 2023
The evolution of the mitochondrial disease diagnostic odysseyJohn L P Thompson, Amel Karaa, Hung Pham, et al.
Pageof 11