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John F Robinson

Showing results (11-20 of 43) with videos related to

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Clinical Biochemistry|August 27, 2004
Optimizing RNA extraction yield from whole blood for microarray gene expression analysisJian Wang, John F Robinson, Hafiz M R Khan, et al.
BMC Medical Imaging|September 2, 2006
Semi-automated segmentation and quantification of adipose tissue in calf and thigh by MRI: a preliminary study in patients with monogenic metabolic syndromeSalam A Al-Attar, Rebecca L Pollex, John F Robinson, et al.
Journal of Community Genetics|November 26, 2022
Cost-effectiveness of a gene sequencing test for Alzheimer's disease in OntarioNicolas Iragorri, Danielle Toccalino, Sujata Mishra, et al.
Journal of Medical Genetics|August 7, 2015
Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostosesSali M K Farhan, Jian Wang, John F Robinson, et al.
BMC Medical Genomics|February 12, 2020
Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemiasJacqueline S Dron, Jian Wang, Adam D McIntyre, et al.
Journal of Human Genetics|October 13, 2006
Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profilesJian Wang, John F Robinson, Caroline H O'Neil, et al.
BMC Medical Imaging|March 14, 2007
Quantitative and qualitative differences in subcutaneous adipose tissue stores across lipodystrophy types shown by magnetic resonance imagingSalam A Al-Attar, Rebecca L Pollex, John F Robinson, et al.
Epilepsia|July 26, 2014
Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxiaSali M K Farhan, Lisa M Murphy, John F Robinson, et al.
Orphanet Journal of Rare Diseases|August 21, 2013
A mutation in the serine protease TMPRSS4 in a novel pediatric neurodegenerative disorderPiya Lahiry, Lemuel Racacho, Jian Wang, et al.
The Canadian Journal of Cardiology|December 6, 2014
A novel LIPE nonsense mutation found using exome sequencing in siblings with late-onset familial partial lipodystrophySali M K Farhan, John F Robinson, Adam D McIntyre, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Clinical Biochemistry|August 27, 2004
Optimizing RNA extraction yield from whole blood for microarray gene expression analysisJian Wang, John F Robinson, Hafiz M R Khan, et al.
BMC Medical Imaging|September 2, 2006
Semi-automated segmentation and quantification of adipose tissue in calf and thigh by MRI: a preliminary study in patients with monogenic metabolic syndromeSalam A Al-Attar, Rebecca L Pollex, John F Robinson, et al.
Journal of Community Genetics|November 26, 2022
Cost-effectiveness of a gene sequencing test for Alzheimer's disease in OntarioNicolas Iragorri, Danielle Toccalino, Sujata Mishra, et al.
Journal of Medical Genetics|August 7, 2015
Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostosesSali M K Farhan, Jian Wang, John F Robinson, et al.
BMC Medical Genomics|February 12, 2020
Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemiasJacqueline S Dron, Jian Wang, Adam D McIntyre, et al.
Journal of Human Genetics|October 13, 2006
Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profilesJian Wang, John F Robinson, Caroline H O'Neil, et al.
BMC Medical Imaging|March 14, 2007
Quantitative and qualitative differences in subcutaneous adipose tissue stores across lipodystrophy types shown by magnetic resonance imagingSalam A Al-Attar, Rebecca L Pollex, John F Robinson, et al.
Epilepsia|July 26, 2014
Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxiaSali M K Farhan, Lisa M Murphy, John F Robinson, et al.
Orphanet Journal of Rare Diseases|August 21, 2013
A mutation in the serine protease TMPRSS4 in a novel pediatric neurodegenerative disorderPiya Lahiry, Lemuel Racacho, Jian Wang, et al.
The Canadian Journal of Cardiology|December 6, 2014
A novel LIPE nonsense mutation found using exome sequencing in siblings with late-onset familial partial lipodystrophySali M K Farhan, John F Robinson, Adam D McIntyre, et al.
Pageof 5