Search research articles
Contact Us
Filters
Showing results (11-20 of 43) with videos related to
Page
of 5
Sort By:
Clinical Biochemistry
|
August 27, 2004
Optimizing RNA extraction yield from whole blood for microarray gene expression analysis
Jian 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 syndrome
Salam 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 Ontario
Nicolas 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 exostoses
Sali 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 dyslipidemias
Jacqueline 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 profiles
Jian 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 imaging
Salam 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 ataxia
Sali 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 disorder
Piya 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 lipodystrophy
Sali M K Farhan, John F Robinson, Adam D McIntyre, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 43) with videos related to
Sort By:
Page
of 5
Clinical Biochemistry
|
August 27, 2004
Optimizing RNA extraction yield from whole blood for microarray gene expression analysis
Jian 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 syndrome
Salam 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 Ontario
Nicolas 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 exostoses
Sali 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 dyslipidemias
Jacqueline 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 profiles
Jian 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 imaging
Salam 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 ataxia
Sali 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 disorder
Piya 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 lipodystrophy
Sali M K Farhan, John F Robinson, Adam D McIntyre, et al.
Page
of 5