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Jennifer Mackenzie

Showing results (21-30 of 32) with videos related to

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The Journal of School Health|November 22, 2021
Implementation of Telehealth Services in Rural Schools: A Qualitative AssessmentKimberley Fox, Amanda Burgess, Martha Elbaum Williamson, et al.
Canadian Family Physician Medecin De Famille Canadien|January 24, 2013
Maternal age-based prenatal screening for chromosomal disorders: attitudes of women and health care providers toward changesJune C Carroll, Andrea Rideout, Brenda J Wilson, et al.
Molecular Genetics and Metabolism|September 13, 2015
Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007-2014)Srinitya Gannavarapu, Chitra Prasad, Jennifer DiRaimo, et al.
Canadian Family Physician Medecin De Famille Canadien|December 17, 2009
Genetic education for primary care providers: improving attitudes, knowledge, and confidenceJune C Carroll, Andrea L Rideout, Brenda J Wilson, et al.
American Journal of Human Genetics|April 1, 2005
Microduplication and triplication of 22q11.2: a highly variable syndromeTwila M Yobb, Martin J Somerville, Lionel Willatt, et al.
Genome Research|February 3, 2005
Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assayPaul Hardenbol, Fuli Yu, John Belmont, et al.
JIMD Reports|February 27, 2015
Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in CanadaMonica F Lamoureux, Kylie Tingley, Jonathan B Kronick, et al.
Molecular Genetics and Metabolism|November 26, 2013
Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoringSylvia Stockler-Ipsiroglu, Clara van Karnebeek, Nicola Longo, et al.
Orphanet Journal of Rare Diseases|January 16, 2020
Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a reviewMichael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pediatrics|July 16, 2021
Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and PhenylketonuriaMichael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
The Journal of School Health|November 22, 2021
Implementation of Telehealth Services in Rural Schools: A Qualitative AssessmentKimberley Fox, Amanda Burgess, Martha Elbaum Williamson, et al.
Canadian Family Physician Medecin De Famille Canadien|January 24, 2013
Maternal age-based prenatal screening for chromosomal disorders: attitudes of women and health care providers toward changesJune C Carroll, Andrea Rideout, Brenda J Wilson, et al.
Molecular Genetics and Metabolism|September 13, 2015
Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007-2014)Srinitya Gannavarapu, Chitra Prasad, Jennifer DiRaimo, et al.
Canadian Family Physician Medecin De Famille Canadien|December 17, 2009
Genetic education for primary care providers: improving attitudes, knowledge, and confidenceJune C Carroll, Andrea L Rideout, Brenda J Wilson, et al.
American Journal of Human Genetics|April 1, 2005
Microduplication and triplication of 22q11.2: a highly variable syndromeTwila M Yobb, Martin J Somerville, Lionel Willatt, et al.
Genome Research|February 3, 2005
Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assayPaul Hardenbol, Fuli Yu, John Belmont, et al.
JIMD Reports|February 27, 2015
Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in CanadaMonica F Lamoureux, Kylie Tingley, Jonathan B Kronick, et al.
Molecular Genetics and Metabolism|November 26, 2013
Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoringSylvia Stockler-Ipsiroglu, Clara van Karnebeek, Nicola Longo, et al.
Orphanet Journal of Rare Diseases|January 16, 2020
Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a reviewMichael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pediatrics|July 16, 2021
Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and PhenylketonuriaMichael Pugliese, Kylie Tingley, Andrea Chow, et al.
Pageof 4