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Nigel P Carter

Nature genetics

Showing results (1-10 of 9) with videos related to

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Nature Genetics|September 2, 2004
As normal as normal can be?Nigel P Carter
Nature Genetics|September 5, 2007
Methods and strategies for analyzing copy number variation using DNA microarraysNigel P Carter
Nature Genetics|December 6, 2005
A high-resolution survey of deletion polymorphism in the human genomeDonald F Conrad, T Daniel Andrews, Nigel P Carter, et al.
Nature Genetics|December 7, 2007
Germline rates of de novo meiotic deletions and duplications causing several genomic disordersDaniel J Turner, Marcos Miretti, Diana Rajan, et al.
Nature Genetics|September 5, 2007
Challenges and standards in integrating surveys of structural variationStephen W Scherer, Charles Lee, Ewan Birney, et al.
Nature Genetics|September 11, 2007
Diet and the evolution of human amylase gene copy number variationGeorge H Perry, Nathaniel J Dominy, Katrina G Claw, et al.
Nature Genetics|October 7, 2008
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosaMai M Abd El-Aziz, Isabel Barragan, Ciara A O'Driscoll, et al.
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
Nature Genetics|April 6, 2010
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencingHansoo Park, Jong-Il Kim, Young Seok Ju, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Nature Genetics|September 2, 2004
As normal as normal can be?Nigel P Carter
Nature Genetics|September 5, 2007
Methods and strategies for analyzing copy number variation using DNA microarraysNigel P Carter
Nature Genetics|December 6, 2005
A high-resolution survey of deletion polymorphism in the human genomeDonald F Conrad, T Daniel Andrews, Nigel P Carter, et al.
Nature Genetics|December 7, 2007
Germline rates of de novo meiotic deletions and duplications causing several genomic disordersDaniel J Turner, Marcos Miretti, Diana Rajan, et al.
Nature Genetics|September 5, 2007
Challenges and standards in integrating surveys of structural variationStephen W Scherer, Charles Lee, Ewan Birney, et al.
Nature Genetics|September 11, 2007
Diet and the evolution of human amylase gene copy number variationGeorge H Perry, Nathaniel J Dominy, Katrina G Claw, et al.
Nature Genetics|October 7, 2008
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosaMai M Abd El-Aziz, Isabel Barragan, Ciara A O'Driscoll, et al.
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
Nature Genetics|April 6, 2010
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencingHansoo Park, Jong-Il Kim, Young Seok Ju, et al.
Pageof 1