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Marsha D Speevak

Showing results (1-10 of 11) with videos related to

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European Journal of Medical Genetics|July 2, 2013
Charcot-Marie-Tooth 1B caused by expansion of a familial myelin protein zero (MPZ) gene duplicationMarsha D Speevak, Sandra A Farrell
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Non-syndromic language delay in a child with disruption in the Protocadherin11X/Y gene pairMarsha D Speevak, Sandra A Farrell
Prenatal Diagnosis|April 19, 2011
The detection of chromosome anomalies by QF-PCR and residual risks as compared to G-banded analysisMarsha D Speevak, Jean McGowan-Jordan, Kathy Chun
Methods in Molecular Biology (Clifton, N.J.)|April 16, 2002
Whole-cell and microcell fusion for the identification of natural regulators of telomeraseHenriette Gourdeau, Marsha D Speevak, Lucie Jetté, et al.
European Journal of Human Genetics : EJHG|December 4, 2003
Alternatively spliced, truncated human BRCA2 isoforms contain a novel coding exonMarsha D Speevak, Sean S Young, Harriet Feilotter, et al.
American Journal of Medical Genetics. Part A|August 12, 2003
Molecular characterization of an inherited ring (19) demonstrating ring openingMarsha D Speevak, Carolin Smart, Lianne Unwin, et al.
Journal of Human Genetics|November 14, 2009
A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch SyndromeSheron Perera, Lily Ramyar, Angie Mitri, et al.
Journal of Medical Genetics|June 5, 2015
Prenatal genomic microarray and sequencing in Canadian medical practice: towards consensusJanet A Buchanan, David Chitayat, Elena Kolomietz, et al.
Clinical Biochemistry|May 11, 2020
Alpha-1-antitrypsin molecular testing in Canada: A seven year, multi-centre comparisonAndre Mattman, Brian M Gilfix, Sharon Xuehui Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)Matthew S Lebo, Kathleen-Rose Zakoor, Kathy Chun, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
European Journal of Medical Genetics|July 2, 2013
Charcot-Marie-Tooth 1B caused by expansion of a familial myelin protein zero (MPZ) gene duplicationMarsha D Speevak, Sandra A Farrell
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Non-syndromic language delay in a child with disruption in the Protocadherin11X/Y gene pairMarsha D Speevak, Sandra A Farrell
Prenatal Diagnosis|April 19, 2011
The detection of chromosome anomalies by QF-PCR and residual risks as compared to G-banded analysisMarsha D Speevak, Jean McGowan-Jordan, Kathy Chun
Methods in Molecular Biology (Clifton, N.J.)|April 16, 2002
Whole-cell and microcell fusion for the identification of natural regulators of telomeraseHenriette Gourdeau, Marsha D Speevak, Lucie Jetté, et al.
European Journal of Human Genetics : EJHG|December 4, 2003
Alternatively spliced, truncated human BRCA2 isoforms contain a novel coding exonMarsha D Speevak, Sean S Young, Harriet Feilotter, et al.
American Journal of Medical Genetics. Part A|August 12, 2003
Molecular characterization of an inherited ring (19) demonstrating ring openingMarsha D Speevak, Carolin Smart, Lianne Unwin, et al.
Journal of Human Genetics|November 14, 2009
A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch SyndromeSheron Perera, Lily Ramyar, Angie Mitri, et al.
Journal of Medical Genetics|June 5, 2015
Prenatal genomic microarray and sequencing in Canadian medical practice: towards consensusJanet A Buchanan, David Chitayat, Elena Kolomietz, et al.
Clinical Biochemistry|May 11, 2020
Alpha-1-antitrypsin molecular testing in Canada: A seven year, multi-centre comparisonAndre Mattman, Brian M Gilfix, Sharon Xuehui Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)Matthew S Lebo, Kathleen-Rose Zakoor, Kathy Chun, et al.
Pageof 2