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Annals of Emergency Medicine
|
August 27, 2018
Young Man With Paraparesis
Eric Rider, Carl A Gold
Molecular Autism
|
April 16, 2015
Mapk/Erk activation in an animal model of social deficits shows a possible link to autism
Alireza Faridar, Dorothy Jones-Davis, Eric Rider, et al.
Plos One
|
April 25, 2013
Quantitative trait loci for interhemispheric commissure development and social behaviors in the BTBR T⁺ tf/J mouse model of autism
Dorothy M Jones-Davis, Mu Yang, Eric Rider, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene
Nathan Osbun, Jiang Li, Mary C O'Driscoll, et al.
Elife
|
May 4, 2021
DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation
Laura Morcom, Timothy J Edwards, Eric Rider, et al.
Plos Genetics
|
October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria
Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Annals of Emergency Medicine
|
August 27, 2018
Young Man With Paraparesis
Eric Rider, Carl A Gold
Molecular Autism
|
April 16, 2015
Mapk/Erk activation in an animal model of social deficits shows a possible link to autism
Alireza Faridar, Dorothy Jones-Davis, Eric Rider, et al.
Plos One
|
April 25, 2013
Quantitative trait loci for interhemispheric commissure development and social behaviors in the BTBR T⁺ tf/J mouse model of autism
Dorothy M Jones-Davis, Mu Yang, Eric Rider, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene
Nathan Osbun, Jiang Li, Mary C O'Driscoll, et al.
Elife
|
May 4, 2021
DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation
Laura Morcom, Timothy J Edwards, Eric Rider, et al.
Plos Genetics
|
October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria
Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
Page
of 1