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Journal of Proteome Research
|
January 20, 2012
Association of medication with the human plasma N-glycome
Radka Saldova, Jennifer E Huffman, Barbara Adamczyk, et al.
Human Mutation
|
October 2, 2004
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome
Alan F Wright, Adam C Reddick, Sharon B Schwartz, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
March 7, 2015
Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study
Michelle Luciano, Victoria Svinti, Archie Campbell, et al.
The New England Journal of Medicine
|
July 20, 2007
Complement C3 variant and the risk of age-related macular degeneration
John R W Yates, Tiina Sepp, Baljinder K Matharu, et al.
Ophthalmology
|
January 27, 2009
Complement component C3 and risk of age-related macular degeneration
Dominiek D G Despriet, Cornelia M van Duijn, Ben A Oostra, et al.
Molecular Vision
|
August 19, 2006
Molecular genetics of retinitis pigmentosa in two Romani (Gypsy) families
Christina F Chakarova, Sylvia Cherninkova, Ivailo Tournev, et al.
Plos One
|
September 3, 2011
Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolates
Wenhua Wei, Gibran Hemani, Andrew A Hicks, et al.
Investigative Ophthalmology & Visual Science
|
July 2, 2010
Complement factor h autoantibodies and age-related macular degeneration
Baljean Dhillon, Alan F Wright, Adnan Tufail, et al.
Croatian Medical Journal
|
March 5, 2009
Genome-wide association study of biochemical traits in Korcula Island, Croatia
Tatijana Zemunik, Mladen Boban, Gordan Lauc, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2012
Genome-wide analysis of epistasis in body mass index using multiple human populations
Wen-Hua Wei, Gib Hemani, Attila Gyenesei, et al.
Page
of 24
Search research articles
Search
Showing results (111-120 of 239) with videos related to
Sort By:
Page
of 24
Journal of Proteome Research
|
January 20, 2012
Association of medication with the human plasma N-glycome
Radka Saldova, Jennifer E Huffman, Barbara Adamczyk, et al.
Human Mutation
|
October 2, 2004
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome
Alan F Wright, Adam C Reddick, Sharon B Schwartz, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
March 7, 2015
Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study
Michelle Luciano, Victoria Svinti, Archie Campbell, et al.
The New England Journal of Medicine
|
July 20, 2007
Complement C3 variant and the risk of age-related macular degeneration
John R W Yates, Tiina Sepp, Baljinder K Matharu, et al.
Ophthalmology
|
January 27, 2009
Complement component C3 and risk of age-related macular degeneration
Dominiek D G Despriet, Cornelia M van Duijn, Ben A Oostra, et al.
Molecular Vision
|
August 19, 2006
Molecular genetics of retinitis pigmentosa in two Romani (Gypsy) families
Christina F Chakarova, Sylvia Cherninkova, Ivailo Tournev, et al.
Plos One
|
September 3, 2011
Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolates
Wenhua Wei, Gibran Hemani, Andrew A Hicks, et al.
Investigative Ophthalmology & Visual Science
|
July 2, 2010
Complement factor h autoantibodies and age-related macular degeneration
Baljean Dhillon, Alan F Wright, Adnan Tufail, et al.
Croatian Medical Journal
|
March 5, 2009
Genome-wide association study of biochemical traits in Korcula Island, Croatia
Tatijana Zemunik, Mladen Boban, Gordan Lauc, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2012
Genome-wide analysis of epistasis in body mass index using multiple human populations
Wen-Hua Wei, Gib Hemani, Attila Gyenesei, et al.
Page
of 24