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American Journal of Medical Genetics. Part A
|
April 27, 2007
A novel VEGFR3 mutation causes Milroy disease
Matthew G Butler, Susan L Dagenais, Stanley G Rockson, et al.
American Journal of Human Genetics
|
August 17, 2004
Chromosomal instability at common fragile sites in Seckel syndrome
Anne M Casper, Sandra G Durkin, Martin F Arlt, et al.
Genes, Chromosomes & Cancer
|
December 18, 2001
Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells
Martin F Arlt, Diane E Miller, David G Beer, et al.
Genes, Chromosomes & Cancer
|
May 15, 2002
Direct correlation between FRA3B expression and cigarette smoking
Constance K Stein, Thomas W Glover, J Lynn Palmer, et al.
Genes, Chromosomes & Cancer
|
July 11, 2008
Stably transfected common fragile site sequences exhibit instability at ectopic sites
Ryan L Ragland, Michael W Glynn, Martin F Arlt, et al.
Human Molecular Genetics
|
October 26, 2005
Mechanisms of common fragile site instability
Thomas W Glover, Martin F Arlt, Anne M Casper, et al.
DNA Repair
|
June 30, 2006
Common fragile sites as targets for chromosome rearrangements
Martin F Arlt, Sandra G Durkin, Ryan L Ragland, et al.
NAR Genomics and Bioinformatics
|
May 14, 2023
svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing
Thomas E Wilson, Samreen Ahmed, Jake Higgins, et al.
Plos Genetics
|
October 3, 2012
De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining
Martin F Arlt, Sountharia Rajendran, Shanda R Birkeland, et al.
Human Molecular Genetics
|
January 22, 2005
The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability
Niall G Howlett, Toshiyasu Taniguchi, Sandra G Durkin, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 56) with videos related to
Sort By:
Page
of 6
American Journal of Medical Genetics. Part A
|
April 27, 2007
A novel VEGFR3 mutation causes Milroy disease
Matthew G Butler, Susan L Dagenais, Stanley G Rockson, et al.
American Journal of Human Genetics
|
August 17, 2004
Chromosomal instability at common fragile sites in Seckel syndrome
Anne M Casper, Sandra G Durkin, Martin F Arlt, et al.
Genes, Chromosomes & Cancer
|
December 18, 2001
Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells
Martin F Arlt, Diane E Miller, David G Beer, et al.
Genes, Chromosomes & Cancer
|
May 15, 2002
Direct correlation between FRA3B expression and cigarette smoking
Constance K Stein, Thomas W Glover, J Lynn Palmer, et al.
Genes, Chromosomes & Cancer
|
July 11, 2008
Stably transfected common fragile site sequences exhibit instability at ectopic sites
Ryan L Ragland, Michael W Glynn, Martin F Arlt, et al.
Human Molecular Genetics
|
October 26, 2005
Mechanisms of common fragile site instability
Thomas W Glover, Martin F Arlt, Anne M Casper, et al.
DNA Repair
|
June 30, 2006
Common fragile sites as targets for chromosome rearrangements
Martin F Arlt, Sandra G Durkin, Ryan L Ragland, et al.
NAR Genomics and Bioinformatics
|
May 14, 2023
svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing
Thomas E Wilson, Samreen Ahmed, Jake Higgins, et al.
Plos Genetics
|
October 3, 2012
De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining
Martin F Arlt, Sountharia Rajendran, Shanda R Birkeland, et al.
Human Molecular Genetics
|
January 22, 2005
The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability
Niall G Howlett, Toshiyasu Taniguchi, Sandra G Durkin, et al.
Page
of 6