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John F Robinson

Showing results (21-30 of 43) with videos related to

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Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|August 13, 2004
Spectrum of HNF1A and GCK mutations in Canadian families with maturity-onset diabetes of the young (MODY)James L McKinney, Henian Cao, John F Robinson, et al.
BMC Medical Genomics|June 5, 2019
Targeted next generation sequencing as a tool for precision medicineMarkus Gulilat, Tyler Lamb, Wendy A Teft, et al.
Journal of Lipid Research|February 8, 2014
LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemiasChristopher T Johansen, Joseph B Dubé, Melissa N Loyzer, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiencySali M K Farhan, Jian Wang, John F Robinson, et al.
Human Genetics|July 5, 2016
Whole-genome sequencing in French Canadians from QuebecCécile Low-Kam, David Rhainds, Ken Sin Lo, et al.
Canadian Journal of Diabetes|October 4, 2020
Simplifying Detection of Copy-Number Variations in Maturity-Onset Diabetes of the YoungAmanda J Berberich, Jian Wang, Henian Cao, et al.
Brain : a Journal of Neurology|October 4, 2019
Genetic and epigenetic study of an Alzheimer's disease family with monozygotic tripletsMing Zhang, Allison A Dilliott, Roaa Khallaf, et al.
RNA Biology|August 14, 2019
Targeted sequencing reveals expanded genetic diversity of human transfer RNAsMatthew D Berg, Daniel J Giguere, Jacqueline S Dron, et al.
The Canadian Journal of Cardiology|October 2, 2018
Whole-Gene Duplication of PCSK9 as a Novel Genetic Mechanism for Severe Familial HypercholesterolemiaMichael A Iacocca, Jian Wang, Samantha Sarkar, et al.
Journal of Lipid Research|September 15, 2019
Partial <i>LPL</i> deletions: rare copy-number variants contributing towards severe hypertriglyceridemiaJacqueline S Dron, Jian Wang, Adam D McIntyre, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|August 13, 2004
Spectrum of HNF1A and GCK mutations in Canadian families with maturity-onset diabetes of the young (MODY)James L McKinney, Henian Cao, John F Robinson, et al.
BMC Medical Genomics|June 5, 2019
Targeted next generation sequencing as a tool for precision medicineMarkus Gulilat, Tyler Lamb, Wendy A Teft, et al.
Journal of Lipid Research|February 8, 2014
LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemiasChristopher T Johansen, Joseph B Dubé, Melissa N Loyzer, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiencySali M K Farhan, Jian Wang, John F Robinson, et al.
Human Genetics|July 5, 2016
Whole-genome sequencing in French Canadians from QuebecCécile Low-Kam, David Rhainds, Ken Sin Lo, et al.
Canadian Journal of Diabetes|October 4, 2020
Simplifying Detection of Copy-Number Variations in Maturity-Onset Diabetes of the YoungAmanda J Berberich, Jian Wang, Henian Cao, et al.
Brain : a Journal of Neurology|October 4, 2019
Genetic and epigenetic study of an Alzheimer's disease family with monozygotic tripletsMing Zhang, Allison A Dilliott, Roaa Khallaf, et al.
RNA Biology|August 14, 2019
Targeted sequencing reveals expanded genetic diversity of human transfer RNAsMatthew D Berg, Daniel J Giguere, Jacqueline S Dron, et al.
The Canadian Journal of Cardiology|October 2, 2018
Whole-Gene Duplication of PCSK9 as a Novel Genetic Mechanism for Severe Familial HypercholesterolemiaMichael A Iacocca, Jian Wang, Samantha Sarkar, et al.
Journal of Lipid Research|September 15, 2019
Partial <i>LPL</i> deletions: rare copy-number variants contributing towards severe hypertriglyceridemiaJacqueline S Dron, Jian Wang, Adam D McIntyre, et al.
Pageof 5