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Pierre Drapeau

Showing results (91-100 of 97) with videos related to

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The New England Journal of Medicine|February 7, 2009
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardationFadi F Hamdan, Julie Gauthier, Dan Spiegelman, et al.
The Journal of Clinical Investigation|February 3, 2015
Functional variants of POC5 identified in patients with idiopathic scoliosisShunmoogum A Patten, Patricia Margaritte-Jeannin, Jean-Claude Bernard, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophreniaJulie Gauthier, Nathalie Champagne, Ronald G Lafrenière, et al.
American Journal of Human Genetics|March 8, 2011
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disabilityFadi F Hamdan, Julie Gauthier, Yoichi Araki, et al.
Zebrafish|June 2, 2016
Restrictions on the Importation of Zebrafish into Canada Associated with Spring Viremia of Carp VirusDavid Hanwell, Sarah A Hutchinson, Chereen Collymore, et al.
American Journal of Human Genetics|August 28, 2010
Direct measure of the de novo mutation rate in autism and schizophrenia cohortsPhilip Awadalla, Julie Gauthier, Rachel A Myers, et al.
Pageof 10

Showing results (91-100 of 97) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 97 results.
The New England Journal of Medicine|February 7, 2009
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardationFadi F Hamdan, Julie Gauthier, Dan Spiegelman, et al.
The Journal of Clinical Investigation|February 3, 2015
Functional variants of POC5 identified in patients with idiopathic scoliosisShunmoogum A Patten, Patricia Margaritte-Jeannin, Jean-Claude Bernard, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophreniaJulie Gauthier, Nathalie Champagne, Ronald G Lafrenière, et al.
American Journal of Human Genetics|March 8, 2011
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disabilityFadi F Hamdan, Julie Gauthier, Yoichi Araki, et al.
Zebrafish|June 2, 2016
Restrictions on the Importation of Zebrafish into Canada Associated with Spring Viremia of Carp VirusDavid Hanwell, Sarah A Hutchinson, Chereen Collymore, et al.
American Journal of Human Genetics|August 28, 2010
Direct measure of the de novo mutation rate in autism and schizophrenia cohortsPhilip Awadalla, Julie Gauthier, Rachel A Myers, et al.
Pageof 10