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Nutrients
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August 10, 2021
Nutrition and Frailty: Opportunities for Prevention and Treatment
Mary Ni Lochlainn, Natalie J Cox, Thomas Wilson, et al.
American Journal of Medical Genetics. Part A
|
December 23, 2022
Detection of mosaic variants using genome sequencing in a large pediatric cohort
Jacqueline A Odgis, Katie M Gallagher, Atteeq U Rehman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 9, 2023
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients
Noura S Abul-Husn, Priya N Marathe, Nicole R Kelly, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 30, 2023
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients
Noura S Abul-Husn, Priya N Marathe, Nicole R Kelly, et al.
The Canadian Journal of Cardiology
|
June 13, 2008
The 2008 Canadian Hypertension Education Program recommendations for the management of hypertension: Part 1 - blood pressure measurement, diagnosis and assessment of risk
Raj S Padwal, Brenda R Hemmelgarn, Nadia A Khan, et al.
The Canadian Journal of Cardiology
|
May 7, 2009
The 2009 Canadian Hypertension Education Program recommendations for the management of hypertension: Part 1--blood pressure measurement, diagnosis and assessment of risk
Raj S Padwal, Brenda R Hemmelgarn, Nadia A Khan, et al.
Clinical Genetics
|
June 19, 2023
Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program
Katherine E Bonini, Amanda Thomas-Wilson, Priya N Marathe, et al.
European Journal of Human Genetics : EJHG
|
July 27, 2023
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays
Mythily Ganapathi, Leticia S Matsuoka, Michael March, et al.
The Canadian Journal of Cardiology
|
May 21, 2010
The 2010 Canadian Hypertension Education Program recommendations for the management of hypertension: part I - blood pressure measurement, diagnosis and assessment of risk
Robert R Quinn, Brenda R Hemmelgarn, Raj S Padwal, et al.
Journal of the Endocrine Society
|
June 8, 2026
Genome sequencing identifies monogenic causes in adults with metabolic diseases
Volkan Okur, Amanda Marcus, John N Falcone, et al.
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of 16
Search research articles
Search
Showing results (141-150 of 155) with videos related to
Sort By:
Page
of 16
Nutrients
|
August 10, 2021
Nutrition and Frailty: Opportunities for Prevention and Treatment
Mary Ni Lochlainn, Natalie J Cox, Thomas Wilson, et al.
American Journal of Medical Genetics. Part A
|
December 23, 2022
Detection of mosaic variants using genome sequencing in a large pediatric cohort
Jacqueline A Odgis, Katie M Gallagher, Atteeq U Rehman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 9, 2023
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients
Noura S Abul-Husn, Priya N Marathe, Nicole R Kelly, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 30, 2023
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients
Noura S Abul-Husn, Priya N Marathe, Nicole R Kelly, et al.
The Canadian Journal of Cardiology
|
June 13, 2008
The 2008 Canadian Hypertension Education Program recommendations for the management of hypertension: Part 1 - blood pressure measurement, diagnosis and assessment of risk
Raj S Padwal, Brenda R Hemmelgarn, Nadia A Khan, et al.
The Canadian Journal of Cardiology
|
May 7, 2009
The 2009 Canadian Hypertension Education Program recommendations for the management of hypertension: Part 1--blood pressure measurement, diagnosis and assessment of risk
Raj S Padwal, Brenda R Hemmelgarn, Nadia A Khan, et al.
Clinical Genetics
|
June 19, 2023
Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program
Katherine E Bonini, Amanda Thomas-Wilson, Priya N Marathe, et al.
European Journal of Human Genetics : EJHG
|
July 27, 2023
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays
Mythily Ganapathi, Leticia S Matsuoka, Michael March, et al.
The Canadian Journal of Cardiology
|
May 21, 2010
The 2010 Canadian Hypertension Education Program recommendations for the management of hypertension: part I - blood pressure measurement, diagnosis and assessment of risk
Robert R Quinn, Brenda R Hemmelgarn, Raj S Padwal, et al.
Journal of the Endocrine Society
|
June 8, 2026
Genome sequencing identifies monogenic causes in adults with metabolic diseases
Volkan Okur, Amanda Marcus, John N Falcone, et al.
Page
of 16