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Laura Arbour

Showing results (71-80 of 118) with videos related to

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Frontiers in Pediatrics|June 17, 2024
A mild phenotype associated with <i>KCNQ1</i> p.V205M mediated long QT syndrome in First Nations children of Northern British Columbia: effect of additional variants and considerations for managementSimona Bene Watts, Barbara Gauthier, Anders C Erickson, et al.
Journal of Medical Genetics|March 8, 2017
KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1Jamie D Kapplinger, Anders Erickson, Sirisha Asuri, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|June 23, 2026
Association between interventional cardiologist practice characteristics, CABG use, and clinical outcomesJustin Blackman, Stephanie Quon, Darrel P Francis, et al.
American Journal of Industrial Medicine|July 8, 2010
Exposure to anesthetic gases and congenital anomalies in offspring of female registered nursesKay Teschke, Zenaida Abanto, Laura Arbour, et al.
Molecular Genetics and Metabolism|August 11, 2010
Carnitine palmitoyltransferase 1A (CPT1A) P479L prevalence in live newborns in Yukon, Northwest Territories, and NunavutSorcha A Collins, Graham Sinclair, Sarah McIntosh, et al.
NPJ Genomic Medicine|September 29, 2025
Biallelic variants in BBOX1 cause L-Carnitine deficiency and elevated γ-butyrobetaineXiao Li, Mehdi Yeganeh, Graham Sinclair, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 21, 2024
Head circumference values among Inuit children in Nunavut, Canada: a retrospective cohort studyKristina May Joyal, Sorcha Collins, Amber Miners, et al.
Frontiers in Pediatrics|July 23, 2021
Association of the <i>CPT1A</i> p.P479L Metabolic Gene Variant With Childhood Respiratory and Other Infectious Illness in NunavutSorcha A Collins, Sharon Edmunds, Gwen Healey Akearok, et al.
American Journal of Medical Genetics. Part A|May 23, 2012
Beckwith-Wiedemann syndrome in sibs discordant for IC2 methylationKaren Y Niederhoffer, Maria Peñaherrera, Denise Pugash, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2026
Forced resilience: Indigenous perspectives on systemic barriers and humanizing genomic medicine in British Columbia, CanadaMorgan Ehman, Laurie Montour, Samantha Pollard, et al.
Pageof 12

Showing results (71-80 of 118) with videos related to

Sort By:
Pageof 12
Frontiers in Pediatrics|June 17, 2024
A mild phenotype associated with <i>KCNQ1</i> p.V205M mediated long QT syndrome in First Nations children of Northern British Columbia: effect of additional variants and considerations for managementSimona Bene Watts, Barbara Gauthier, Anders C Erickson, et al.
Journal of Medical Genetics|March 8, 2017
KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1Jamie D Kapplinger, Anders Erickson, Sirisha Asuri, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|June 23, 2026
Association between interventional cardiologist practice characteristics, CABG use, and clinical outcomesJustin Blackman, Stephanie Quon, Darrel P Francis, et al.
American Journal of Industrial Medicine|July 8, 2010
Exposure to anesthetic gases and congenital anomalies in offspring of female registered nursesKay Teschke, Zenaida Abanto, Laura Arbour, et al.
Molecular Genetics and Metabolism|August 11, 2010
Carnitine palmitoyltransferase 1A (CPT1A) P479L prevalence in live newborns in Yukon, Northwest Territories, and NunavutSorcha A Collins, Graham Sinclair, Sarah McIntosh, et al.
NPJ Genomic Medicine|September 29, 2025
Biallelic variants in BBOX1 cause L-Carnitine deficiency and elevated γ-butyrobetaineXiao Li, Mehdi Yeganeh, Graham Sinclair, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 21, 2024
Head circumference values among Inuit children in Nunavut, Canada: a retrospective cohort studyKristina May Joyal, Sorcha Collins, Amber Miners, et al.
Frontiers in Pediatrics|July 23, 2021
Association of the <i>CPT1A</i> p.P479L Metabolic Gene Variant With Childhood Respiratory and Other Infectious Illness in NunavutSorcha A Collins, Sharon Edmunds, Gwen Healey Akearok, et al.
American Journal of Medical Genetics. Part A|May 23, 2012
Beckwith-Wiedemann syndrome in sibs discordant for IC2 methylationKaren Y Niederhoffer, Maria Peñaherrera, Denise Pugash, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2026
Forced resilience: Indigenous perspectives on systemic barriers and humanizing genomic medicine in British Columbia, CanadaMorgan Ehman, Laurie Montour, Samantha Pollard, et al.
Pageof 12