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Human Mutation
|
March 20, 2008
K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population
Ron Do, Guillaume Paré, Alexandre Montpetit, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 30, 2004
Association of vitamin D receptor genetic variants with susceptibility to asthma and atopy
Audrey H Poon, Catherine Laprise, Mathieu Lemire, et al.
The Journal of Gene Medicine
|
September 29, 2011
Endonucleases: tools to correct the dystrophin gene
Joel Rousseau, Pierre Chapdelaine, Sébastien Boisvert, et al.
Pediatric Research
|
March 24, 2010
Newborn serum retinoic acid level is associated with variants of genes in the retinol metabolism pathway
Daniel C Manolescu, Reyhan El-Kares, Lajmi Lakhal-Chaieb, et al.
Human Genetics
|
January 26, 2005
An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22
Thomas G Saba, Alexandre Montpetit, Andrei Verner, et al.
Diabetes
|
December 29, 2006
Genetic control of alternative splicing in the TAP2 gene: possible implication in the genetics of type 1 diabetes
Hui-Qi Qu, Yang Lu, Luc Marchand, et al.
Human Pathology
|
May 21, 2009
SNP genotyping of a sclerosing rhabdomyosarcoma: reveals highly aneuploid profile and a specific MDM2/HMGA2 amplification
Dorothée Bouron-Dal Soglio, Anne-Laure Rougemont, Riwa Absi, et al.
Kidney International
|
April 9, 2010
A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid
Reyhan El Kares, Daniel C Manolescu, Lajmi Lakhal-Chaieb, et al.
Plos One
|
January 16, 2008
Correction of population stratification in large multi-ethnic association studies
David Serre, Alexandre Montpetit, Guillaume Paré, et al.
Plos Genetics
|
March 15, 2006
An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population
Alexandre Montpetit, Mari Nelis, Philippe Laflamme, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 92) with videos related to
Sort By:
Page
of 10
Human Mutation
|
March 20, 2008
K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population
Ron Do, Guillaume Paré, Alexandre Montpetit, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 30, 2004
Association of vitamin D receptor genetic variants with susceptibility to asthma and atopy
Audrey H Poon, Catherine Laprise, Mathieu Lemire, et al.
The Journal of Gene Medicine
|
September 29, 2011
Endonucleases: tools to correct the dystrophin gene
Joel Rousseau, Pierre Chapdelaine, Sébastien Boisvert, et al.
Pediatric Research
|
March 24, 2010
Newborn serum retinoic acid level is associated with variants of genes in the retinol metabolism pathway
Daniel C Manolescu, Reyhan El-Kares, Lajmi Lakhal-Chaieb, et al.
Human Genetics
|
January 26, 2005
An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22
Thomas G Saba, Alexandre Montpetit, Andrei Verner, et al.
Diabetes
|
December 29, 2006
Genetic control of alternative splicing in the TAP2 gene: possible implication in the genetics of type 1 diabetes
Hui-Qi Qu, Yang Lu, Luc Marchand, et al.
Human Pathology
|
May 21, 2009
SNP genotyping of a sclerosing rhabdomyosarcoma: reveals highly aneuploid profile and a specific MDM2/HMGA2 amplification
Dorothée Bouron-Dal Soglio, Anne-Laure Rougemont, Riwa Absi, et al.
Kidney International
|
April 9, 2010
A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid
Reyhan El Kares, Daniel C Manolescu, Lajmi Lakhal-Chaieb, et al.
Plos One
|
January 16, 2008
Correction of population stratification in large multi-ethnic association studies
David Serre, Alexandre Montpetit, Guillaume Paré, et al.
Plos Genetics
|
March 15, 2006
An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population
Alexandre Montpetit, Mari Nelis, Philippe Laflamme, et al.
Page
of 10