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Marsha Speevak

Showing results (1-10 of 14) with videos related to

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BMJ Case Reports|November 14, 2014
A fourth case of Feingold syndrome type 2: psychiatric presentation and managementHooman Ganjavi, Victoria Mok Siu, Marsha Speevak, et al.
Journal of Medical Genetics|July 14, 2019
CCMG practice guideline: laboratory guidelines for next-generation sequencingStacey Hume, Tanya N Nelson, Marsha Speevak, et al.
Clinical Biochemistry|February 23, 2020
Null<sub>Canada</sub>: A novel α<sub>1</sub>-antitrypsin allele with in cis variants Glu366Lys and Ile100AsnSharon Chen, Mari L DeMarco, Mathew P Estey, et al.
American Journal of Medical Genetics. Part A|July 28, 2022
Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplicationIrene E Drmic, Bonnie MacKinnon Modi, Beth McConnell, et al.
Genome Medicine|December 1, 2017
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophreniaChelsea Lowther, Daniele Merico, Gregory Costain, et al.
Molecular Diagnosis & Therapy|October 4, 2022
Prevalence of NTRK Fusions in Canadian Solid Tumour Cancer PatientsJoshua D Silvertown, Connie Lisle, Laura Semenuk, et al.
American Journal of Medical Genetics. Part A|May 7, 2015
Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric populationBita Hashemi, Anne Bassett, David Chitayat, et al.
Human Molecular Genetics|July 2, 2013
Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarraysGregory Costain, Anath C Lionel, Daniele Merico, et al.
JTO Clinical and Research Reports|September 30, 2021
A Pan-Canadian Validation Study for the Detection of <i>EGFR</i> T790M Mutation Using Circulating Tumor DNA From Peripheral BloodShamini Selvarajah, Sophie Plante, Marsha Speevak, et al.
American Journal of Human Genetics|February 4, 2018
OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion SyndromeMohammed Uddin, Brianna K Unda, Vickie Kwan, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
BMJ Case Reports|November 14, 2014
A fourth case of Feingold syndrome type 2: psychiatric presentation and managementHooman Ganjavi, Victoria Mok Siu, Marsha Speevak, et al.
Journal of Medical Genetics|July 14, 2019
CCMG practice guideline: laboratory guidelines for next-generation sequencingStacey Hume, Tanya N Nelson, Marsha Speevak, et al.
Clinical Biochemistry|February 23, 2020
Null<sub>Canada</sub>: A novel α<sub>1</sub>-antitrypsin allele with in cis variants Glu366Lys and Ile100AsnSharon Chen, Mari L DeMarco, Mathew P Estey, et al.
American Journal of Medical Genetics. Part A|July 28, 2022
Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplicationIrene E Drmic, Bonnie MacKinnon Modi, Beth McConnell, et al.
Genome Medicine|December 1, 2017
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophreniaChelsea Lowther, Daniele Merico, Gregory Costain, et al.
Molecular Diagnosis & Therapy|October 4, 2022
Prevalence of NTRK Fusions in Canadian Solid Tumour Cancer PatientsJoshua D Silvertown, Connie Lisle, Laura Semenuk, et al.
American Journal of Medical Genetics. Part A|May 7, 2015
Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric populationBita Hashemi, Anne Bassett, David Chitayat, et al.
Human Molecular Genetics|July 2, 2013
Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarraysGregory Costain, Anath C Lionel, Daniele Merico, et al.
JTO Clinical and Research Reports|September 30, 2021
A Pan-Canadian Validation Study for the Detection of <i>EGFR</i> T790M Mutation Using Circulating Tumor DNA From Peripheral BloodShamini Selvarajah, Sophie Plante, Marsha Speevak, et al.
American Journal of Human Genetics|February 4, 2018
OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion SyndromeMohammed Uddin, Brianna K Unda, Vickie Kwan, et al.
Pageof 2