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The Canadian Journal of Cardiology
|
November 29, 2011
How much is enough? Weighing the evidence for mutation pathogenicity
Tara L Dzwiniel, Dawna M Gilchrist, Stacey Hume
Ophthalmic Genetics
|
January 1, 2013
Copy number variant analysis in CHM to detect duplications underlying choroideremia
Jonathan Y Chi, Ian M MacDonald, Stacey Hume
Journal of Genetic Counseling
|
November 15, 2011
Defining the role of laboratory genetic counselor
Susan Christian, Margaret Lilley, Stacey Hume, et al.
Molecular Genetics and Metabolism
|
October 27, 2018
Plasma-derived cell-free mitochondrial DNA: A novel non-invasive methodology to identify mitochondrial DNA haplogroups in humans
Christopher Newell, Stacey Hume, Steven C Greenway, et al.
Pharmacogenetics and Genomics
|
August 23, 2020
Identification of high-impact gene-drug pairs for pharmacogenetic testing in Alberta, Canada
Mikayla Fan, Mark C Yarema, Adrian Box, et al.
Prenatal Diagnosis
|
July 9, 2017
Assessing the cost of implementing the 2011 Society of Obstetricians and Gynecologists of Canada and Canadian College of Medical Genetics practice guidelines on the detection of fetal aneuploidies
Margaret Lilley, Stacey Hume, Nina Karpoff, et al.
American Journal of Medical Genetics. Part A
|
February 19, 2026
Identification of Two Novel Mutations in the CHM Gene Causing Choroideremia
Farshad Niri, Alina Radziwon, Rachel Mah, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC
|
July 23, 2017
Mitochondrial Replacement Therapy: The Road to the Clinic in Canada
Bartha Maria Knoppers, Arthur Leader, Stacey Hume, et al.
Paediatrics & Child Health
|
November 2, 2011
Newborn screening for cystic fibrosis in Alberta: Two years of experience
Margaret Lilley, Susan Christian, Stacey Hume, et al.
Neurology. Genetics
|
June 14, 2019
Hybrid gel electrophoresis using skin fibroblasts to aid in diagnosing mitochondrial disease
Christopher Newell, Aneal Khan, David Sinasac, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
The Canadian Journal of Cardiology
|
November 29, 2011
How much is enough? Weighing the evidence for mutation pathogenicity
Tara L Dzwiniel, Dawna M Gilchrist, Stacey Hume
Ophthalmic Genetics
|
January 1, 2013
Copy number variant analysis in CHM to detect duplications underlying choroideremia
Jonathan Y Chi, Ian M MacDonald, Stacey Hume
Journal of Genetic Counseling
|
November 15, 2011
Defining the role of laboratory genetic counselor
Susan Christian, Margaret Lilley, Stacey Hume, et al.
Molecular Genetics and Metabolism
|
October 27, 2018
Plasma-derived cell-free mitochondrial DNA: A novel non-invasive methodology to identify mitochondrial DNA haplogroups in humans
Christopher Newell, Stacey Hume, Steven C Greenway, et al.
Pharmacogenetics and Genomics
|
August 23, 2020
Identification of high-impact gene-drug pairs for pharmacogenetic testing in Alberta, Canada
Mikayla Fan, Mark C Yarema, Adrian Box, et al.
Prenatal Diagnosis
|
July 9, 2017
Assessing the cost of implementing the 2011 Society of Obstetricians and Gynecologists of Canada and Canadian College of Medical Genetics practice guidelines on the detection of fetal aneuploidies
Margaret Lilley, Stacey Hume, Nina Karpoff, et al.
American Journal of Medical Genetics. Part A
|
February 19, 2026
Identification of Two Novel Mutations in the CHM Gene Causing Choroideremia
Farshad Niri, Alina Radziwon, Rachel Mah, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC
|
July 23, 2017
Mitochondrial Replacement Therapy: The Road to the Clinic in Canada
Bartha Maria Knoppers, Arthur Leader, Stacey Hume, et al.
Paediatrics & Child Health
|
November 2, 2011
Newborn screening for cystic fibrosis in Alberta: Two years of experience
Margaret Lilley, Susan Christian, Stacey Hume, et al.
Neurology. Genetics
|
June 14, 2019
Hybrid gel electrophoresis using skin fibroblasts to aid in diagnosing mitochondrial disease
Christopher Newell, Aneal Khan, David Sinasac, et al.
Page
of 3