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Andrew R Carson

Showing results (21-30 of 27) with videos related to

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Science Translational Medicine|August 12, 2011
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHDAnath C Lionel, Jennifer Crosbie, Nicole Barbosa, et al.
Annals of Neurology|April 5, 2014
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymiaYing-Zhang Chen, Jennifer R Friedman, Dong-Hui Chen, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, et al.
Science (New York, N.Y.)|April 12, 2003
Human chromosome 7: DNA sequence and biologyStephen W Scherer, Joseph Cheung, Jeffrey R MacDonald, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Science Translational Medicine|August 12, 2011
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHDAnath C Lionel, Jennifer Crosbie, Nicole Barbosa, et al.
Annals of Neurology|April 5, 2014
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymiaYing-Zhang Chen, Jennifer R Friedman, Dong-Hui Chen, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, et al.
Science (New York, N.Y.)|April 12, 2003
Human chromosome 7: DNA sequence and biologyStephen W Scherer, Joseph Cheung, Jeffrey R MacDonald, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
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