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NPJ Genomic Medicine
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May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
Nathaly 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 disease
Nathaly 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 care
Lori A Orlando, R Ryanne Wu, Rachel A Myers, et al.
Human Genetics
|
August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: Citrullinaemia
David 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 disorders
Kristen M Wigby, Deanna Brockman, Gregory Costain, et al.
Human Genetics
|
August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: Citrullinaemia
David 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 activities
R 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 carcinogenesis
Shiran Rabinovich, Alon Silberman, Lital Adler, et al.
Orphanet Journal of Rare Diseases
|
July 20, 2023
Correction to: The evolution of the mitochondrial disease diagnostic odyssey
John L P Thompson, Amel Karaa, Hung Pham, et al.
Orphanet Journal of Rare Diseases
|
June 22, 2023
The evolution of the mitochondrial disease diagnostic odyssey
John L P Thompson, Amel Karaa, Hung Pham, et al.
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of 11
Search research articles
Search
Showing results (51-60 of 101) with videos related to
Sort By:
Page
of 11
NPJ Genomic Medicine
|
May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
Nathaly 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 disease
Nathaly 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 care
Lori A Orlando, R Ryanne Wu, Rachel A Myers, et al.
Human Genetics
|
August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: Citrullinaemia
David 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 disorders
Kristen M Wigby, Deanna Brockman, Gregory Costain, et al.
Human Genetics
|
August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: Citrullinaemia
David 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 activities
R 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 carcinogenesis
Shiran Rabinovich, Alon Silberman, Lital Adler, et al.
Orphanet Journal of Rare Diseases
|
July 20, 2023
Correction to: The evolution of the mitochondrial disease diagnostic odyssey
John L P Thompson, Amel Karaa, Hung Pham, et al.
Orphanet Journal of Rare Diseases
|
June 22, 2023
The evolution of the mitochondrial disease diagnostic odyssey
John L P Thompson, Amel Karaa, Hung Pham, et al.
Page
of 11