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Anne-Marie Laberge

Showing results (51-60 of 93) with videos related to

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Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|February 11, 2019
Canadian Pregnant Women's Preferences Regarding NIPT for Down Syndrome: The Information They Want, How They Want to Get It, and With Whom They Want to Discuss ItAnne-Marie Laberge, Stanislav Birko, Marie-Ève Lemoine, et al.
Journal of Medical Genetics|April 29, 2021
Genetic burden linked to founder effects in Saguenay-Lac-Saint-Jean illustrates the importance of genetic screening test availabilityMbarka Bchetnia, Luigi Bouchard, Jean Mathieu, et al.
Journal of Medical Genetics|August 24, 2025
Reproductive carrier screening for genetic disorders: position statement of the Canadian College of Medical GeneticistsRitu B Aul, Karen Elizabeth Canales, Isabelle De Bie, et al.
Archives of Internal Medicine|January 14, 2009
Motivating factors for physician ordering of factor V Leiden genetic testsLucia A Hindorff, Wylie Burke, Anne-Marie Laberge, et al.
American Journal of Human Genetics|June 15, 2005
A "Fille du Roy" introduced the T14484C Leber hereditary optic neuropathy mutation in French CanadiansAnne-Marie Laberge, Michele Jomphe, Louis Houde, et al.
JIMD Reports|March 13, 2015
Normal Cerebrospinal Fluid Pyridoxal 5'-Phosphate Level in a PNPO-Deficient Patient with Neonatal-Onset Epileptic EncephalopathyAlina Levtova, Stephane Camuzeaux, Anne-Marie Laberge, et al.
BMC Pediatrics|July 21, 2018
The CANadian Pediatric Weight management Registry (CANPWR): lessons learned from developing and initiating a national, multi-centre study embedded in pediatric clinical practiceKatherine M Morrison, Geoff D C Ball, Josephine Ho, et al.
American Journal of Medical Genetics. Part A|December 28, 2019
Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcomeGabrielle T Lemire, Éliane Beauregard-Lacroix, Philippe M Campeau, et al.
International Journal of Neonatal Screening|October 24, 2025
Quebec Spinal Muscular Atrophy Newborn Screening Program: The First Year ExperienceEmilie Groulx-Boivin, Ariane Belzile, Cam-Tu Émilie Nguyen, et al.
Scientific Reports|February 12, 2025
Genome-wide profiling of circulating microRNAs in adolescent idiopathic scoliosis and their relation to spinal deformity severity, and disease pathophysiologyNasrin Khatami, Iurie Caraus, Mahamuda Rahaman, et al.
Pageof 10

Showing results (51-60 of 93) with videos related to

Sort By:
Pageof 10
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|February 11, 2019
Canadian Pregnant Women's Preferences Regarding NIPT for Down Syndrome: The Information They Want, How They Want to Get It, and With Whom They Want to Discuss ItAnne-Marie Laberge, Stanislav Birko, Marie-Ève Lemoine, et al.
Journal of Medical Genetics|April 29, 2021
Genetic burden linked to founder effects in Saguenay-Lac-Saint-Jean illustrates the importance of genetic screening test availabilityMbarka Bchetnia, Luigi Bouchard, Jean Mathieu, et al.
Journal of Medical Genetics|August 24, 2025
Reproductive carrier screening for genetic disorders: position statement of the Canadian College of Medical GeneticistsRitu B Aul, Karen Elizabeth Canales, Isabelle De Bie, et al.
Archives of Internal Medicine|January 14, 2009
Motivating factors for physician ordering of factor V Leiden genetic testsLucia A Hindorff, Wylie Burke, Anne-Marie Laberge, et al.
American Journal of Human Genetics|June 15, 2005
A "Fille du Roy" introduced the T14484C Leber hereditary optic neuropathy mutation in French CanadiansAnne-Marie Laberge, Michele Jomphe, Louis Houde, et al.
JIMD Reports|March 13, 2015
Normal Cerebrospinal Fluid Pyridoxal 5'-Phosphate Level in a PNPO-Deficient Patient with Neonatal-Onset Epileptic EncephalopathyAlina Levtova, Stephane Camuzeaux, Anne-Marie Laberge, et al.
BMC Pediatrics|July 21, 2018
The CANadian Pediatric Weight management Registry (CANPWR): lessons learned from developing and initiating a national, multi-centre study embedded in pediatric clinical practiceKatherine M Morrison, Geoff D C Ball, Josephine Ho, et al.
American Journal of Medical Genetics. Part A|December 28, 2019
Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcomeGabrielle T Lemire, Éliane Beauregard-Lacroix, Philippe M Campeau, et al.
International Journal of Neonatal Screening|October 24, 2025
Quebec Spinal Muscular Atrophy Newborn Screening Program: The First Year ExperienceEmilie Groulx-Boivin, Ariane Belzile, Cam-Tu Émilie Nguyen, et al.
Scientific Reports|February 12, 2025
Genome-wide profiling of circulating microRNAs in adolescent idiopathic scoliosis and their relation to spinal deformity severity, and disease pathophysiologyNasrin Khatami, Iurie Caraus, Mahamuda Rahaman, et al.
Pageof 10