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Methods in Molecular Biology (Clifton, N.J.)
|
January 10, 2012
Structural variation in subtelomeres
M Katharine Rudd
Trends in Genetics : TIG
|
July 26, 2015
Human Structural Variation: Mechanisms of Chromosome Rearrangements
Brooke Weckselblatt, M Katharine Rudd
Clinical Chemistry
|
January 3, 2025
Structural Variation Interpretation in the Genome Sequencing Era: Lessons from Cytogenetics
Lucilla Pizzo, M Katharine Rudd
Trends in Genetics : TIG
|
October 12, 2004
Analysis of the centromeric regions of the human genome assembly
M Katharine Rudd, Huntington F Willard
Genome Research
|
June 14, 2015
Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis
Brooke Weckselblatt, Karen E Hermetz, M Katharine Rudd
Genome Research
|
December 14, 2005
The evolutionary dynamics of alpha-satellite
M Katharine Rudd, Gregory A Wray, Huntington F Willard
American Journal of Human Genetics
|
February 3, 2015
Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints
Scott Newman, Karen E Hermetz, Brooke Weckselblatt, et al.
Molecular and Cellular Biology
|
October 16, 2003
Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag
M Katharine Rudd, Robert W Mays, Stuart Schwartz, et al.
Molecular Cytogenetics
|
January 21, 2012
A recurrent translocation is mediated by homologous recombination between HERV-H elements
Karen E Hermetz, Urvashi Surti, Jannine D Cody, et al.
Plos One
|
July 2, 2014
Tandem repeats and G-rich sequences are enriched at human CNV breakpoints
Promita Bose, Karen E Hermetz, Karen N Conneely, et al.
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of 4
Search research articles
Search
Showing results (1-10 of 35) with videos related to
Sort By:
Page
of 4
Methods in Molecular Biology (Clifton, N.J.)
|
January 10, 2012
Structural variation in subtelomeres
M Katharine Rudd
Trends in Genetics : TIG
|
July 26, 2015
Human Structural Variation: Mechanisms of Chromosome Rearrangements
Brooke Weckselblatt, M Katharine Rudd
Clinical Chemistry
|
January 3, 2025
Structural Variation Interpretation in the Genome Sequencing Era: Lessons from Cytogenetics
Lucilla Pizzo, M Katharine Rudd
Trends in Genetics : TIG
|
October 12, 2004
Analysis of the centromeric regions of the human genome assembly
M Katharine Rudd, Huntington F Willard
Genome Research
|
June 14, 2015
Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis
Brooke Weckselblatt, Karen E Hermetz, M Katharine Rudd
Genome Research
|
December 14, 2005
The evolutionary dynamics of alpha-satellite
M Katharine Rudd, Gregory A Wray, Huntington F Willard
American Journal of Human Genetics
|
February 3, 2015
Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints
Scott Newman, Karen E Hermetz, Brooke Weckselblatt, et al.
Molecular and Cellular Biology
|
October 16, 2003
Human artificial chromosomes with alpha satellite-based de novo centromeres show increased frequency of nondisjunction and anaphase lag
M Katharine Rudd, Robert W Mays, Stuart Schwartz, et al.
Molecular Cytogenetics
|
January 21, 2012
A recurrent translocation is mediated by homologous recombination between HERV-H elements
Karen E Hermetz, Urvashi Surti, Jannine D Cody, et al.
Plos One
|
July 2, 2014
Tandem repeats and G-rich sequences are enriched at human CNV breakpoints
Promita Bose, Karen E Hermetz, Karen N Conneely, et al.
Page
of 4