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Bioinformatics (Oxford, England)
|
September 24, 2005
SNPselector: a web tool for selecting SNPs for genetic association studies
Hong Xu, Simon G Gregory, Elizabeth R Hauser, et al.
American Journal of Human Genetics
|
February 7, 2008
Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein
Gaofeng Wang, Joelle M van der Walt, Gregory Mayhew, et al.
Journal of Pediatric Hematology/Oncology
|
February 9, 2021
Successful Management of Catastrophic Thrombotic Storm in a Young Boy: A Case Report From Northern India
Ankur K Jindal, Jasmina Ahluwalia, Rajiv Suku, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland
|
June 22, 2011
The first 3 years of national bowel cancer screening at a single UK tertiary centre
S Gupta, B P Saunders, C Fraser, et al.
Genomics
|
April 7, 1999
A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequences
S K Horrigan, L Bartoloni, M C Speer, et al.
Muscle & Nerve
|
June 1, 1983
Recombinant DNA strategies in genetic neurological diseases
A D Roses, M A Pericak-Vance, L H Yamaoka, et al.
The British Journal of Ophthalmology
|
May 29, 1998
Coexistence of macular corneal dystrophy types I and II in a single sibship
N P Liu, J Baldwin, F Lennon, et al.
Journal of Neurology
|
January 25, 2011
Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2
Donald S McCorquodale, Gladys Montenegro, Ainsley Peguero, et al.
Cartilage
|
April 6, 2016
Regional Differential Genetic Response of Human Articular Cartilage to Impact Injury
Lauren L Vernon, Danica D Vance, Liyong Wang, et al.
Neurogenetics
|
March 25, 2000
Further exclusion of FSHD1B from the telomeric region of 10q
M C Speer, M A Pericak-Vance, J M Stajich, et al.
Page
of 47
Search research articles
Search
Showing results (161-170 of 466) with videos related to
Sort By:
Page
of 47
Bioinformatics (Oxford, England)
|
September 24, 2005
SNPselector: a web tool for selecting SNPs for genetic association studies
Hong Xu, Simon G Gregory, Elizabeth R Hauser, et al.
American Journal of Human Genetics
|
February 7, 2008
Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein
Gaofeng Wang, Joelle M van der Walt, Gregory Mayhew, et al.
Journal of Pediatric Hematology/Oncology
|
February 9, 2021
Successful Management of Catastrophic Thrombotic Storm in a Young Boy: A Case Report From Northern India
Ankur K Jindal, Jasmina Ahluwalia, Rajiv Suku, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland
|
June 22, 2011
The first 3 years of national bowel cancer screening at a single UK tertiary centre
S Gupta, B P Saunders, C Fraser, et al.
Genomics
|
April 7, 1999
A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequences
S K Horrigan, L Bartoloni, M C Speer, et al.
Muscle & Nerve
|
June 1, 1983
Recombinant DNA strategies in genetic neurological diseases
A D Roses, M A Pericak-Vance, L H Yamaoka, et al.
The British Journal of Ophthalmology
|
May 29, 1998
Coexistence of macular corneal dystrophy types I and II in a single sibship
N P Liu, J Baldwin, F Lennon, et al.
Journal of Neurology
|
January 25, 2011
Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2
Donald S McCorquodale, Gladys Montenegro, Ainsley Peguero, et al.
Cartilage
|
April 6, 2016
Regional Differential Genetic Response of Human Articular Cartilage to Impact Injury
Lauren L Vernon, Danica D Vance, Liyong Wang, et al.
Neurogenetics
|
March 25, 2000
Further exclusion of FSHD1B from the telomeric region of 10q
M C Speer, M A Pericak-Vance, J M Stajich, et al.
Page
of 47