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Nigel P Carter

Showing results (91-100 of 104) with videos related to

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Lancet (London, England)|December 23, 2014
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research dataCaroline F Wright, Tomas W Fitzgerald, Wendy D Jones, et al.
Cell|January 11, 2011
Massive genomic rearrangement acquired in a single catastrophic event during cancer developmentPhilip J Stephens, Chris D Greenman, Beiyuan Fu, et al.
American Journal of Human Genetics|May 15, 2010
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesDavid T Miller, Margaret P Adam, Swaroop Aradhya, et al.
American Journal of Human Genetics|June 9, 2009
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformationsPaweł Stankiewicz, Partha Sen, Samarth S Bhatt, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Cell|February 21, 2012
Genome sequencing and analysis of the Tasmanian devil and its transmissible cancerElizabeth P Murchison, Ole B Schulz-Trieglaff, Zemin Ning, et al.
Nature|September 11, 2009
Prepublication data sharing, Ewan Birney, Thomas J Hudson, et al.
Nature|April 19, 2013
The zebrafish reference genome sequence and its relationship to the human genomeKerstin Howe, Matthew D Clark, Carlos F Torroja, et al.
Nature|November 7, 2008
Accurate whole human genome sequencing using reversible terminator chemistryDavid R Bentley, Shankar Balasubramanian, Harold P Swerdlow, et al.
Nature|April 3, 2010
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls, Nick Craddock, Matthew E Hurles, et al.
Pageof 11

Showing results (91-100 of 104) with videos related to

Sort By:
Pageof 11
Lancet (London, England)|December 23, 2014
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research dataCaroline F Wright, Tomas W Fitzgerald, Wendy D Jones, et al.
Cell|January 11, 2011
Massive genomic rearrangement acquired in a single catastrophic event during cancer developmentPhilip J Stephens, Chris D Greenman, Beiyuan Fu, et al.
American Journal of Human Genetics|May 15, 2010
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesDavid T Miller, Margaret P Adam, Swaroop Aradhya, et al.
American Journal of Human Genetics|June 9, 2009
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformationsPaweł Stankiewicz, Partha Sen, Samarth S Bhatt, et al.
Nature|November 24, 2006
Global variation in copy number in the human genomeRichard Redon, Shumpei Ishikawa, Karen R Fitch, et al.
Cell|February 21, 2012
Genome sequencing and analysis of the Tasmanian devil and its transmissible cancerElizabeth P Murchison, Ole B Schulz-Trieglaff, Zemin Ning, et al.
Nature|September 11, 2009
Prepublication data sharing, Ewan Birney, Thomas J Hudson, et al.
Nature|April 19, 2013
The zebrafish reference genome sequence and its relationship to the human genomeKerstin Howe, Matthew D Clark, Carlos F Torroja, et al.
Nature|November 7, 2008
Accurate whole human genome sequencing using reversible terminator chemistryDavid R Bentley, Shankar Balasubramanian, Harold P Swerdlow, et al.
Nature|April 3, 2010
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls, Nick Craddock, Matthew E Hurles, et al.
Pageof 11