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Human Mutation
|
August 18, 2009
Closely spaced multiple mutations as potential signatures of transient hypermutability in human genes
Jian-Min Chen, Claude Férec, David N Cooper
Genomic Medicine
|
October 17, 2008
Mechanism of Alu integration into the human genome
Jian-Min Chen, Claude Férec, David N Cooper
Public Health Genomics
|
November 30, 2016
The Rise and Rise of Exome Sequencing
Chee-Seng Ku, David N Cooper, George P Patrinos
Human Genetics
|
February 19, 2017
Emerging genotype-phenotype relationships in patients with large NF1 deletions
Hildegard Kehrer-Sawatzki, Victor-Felix Mautner, David N Cooper
Journal of Medical Genetics
|
February 12, 2013
From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic disease
Chee-Seng Ku, Eng King Tan, David N Cooper
Expert Review of Molecular Diagnostics
|
May 24, 2012
The 'sequence everything' approach and personalized clinical decision challenges
Chee-Seng Ku, David N Cooper, Dimitrios H Roukos
Human Genomics
|
September 5, 2015
Trans-species polymorphism in humans and the great apes is generally maintained by balancing selection that modulates the host immune response
Luisa Azevedo, Catarina Serrano, Antonio Amorim, et al.
Methods in Molecular Medicine
|
January 22, 2004
Neurofibromatosis type 1: a common familial cancer syndrome
Meena Upadhyaya, Peter Thompson, Song Han, et al.
Current Protocols in Bioinformatics
|
April 23, 2008
The Human Gene Mutation Database (HGMD) and its exploitation in the study of mutational mechanisms
David N Cooper, Peter D Stenson, Nadia A Chuzhanova
World Journal of Gastroenterology
|
April 20, 2013
Clinical relevance of cancer genome sequencing
Chee Seng Ku, David N Cooper, Dimitrios H Roukos
Page
of 40
Search research articles
Search
Showing results (41-50 of 398) with videos related to
Sort By:
Page
of 40
Human Mutation
|
August 18, 2009
Closely spaced multiple mutations as potential signatures of transient hypermutability in human genes
Jian-Min Chen, Claude Férec, David N Cooper
Genomic Medicine
|
October 17, 2008
Mechanism of Alu integration into the human genome
Jian-Min Chen, Claude Férec, David N Cooper
Public Health Genomics
|
November 30, 2016
The Rise and Rise of Exome Sequencing
Chee-Seng Ku, David N Cooper, George P Patrinos
Human Genetics
|
February 19, 2017
Emerging genotype-phenotype relationships in patients with large NF1 deletions
Hildegard Kehrer-Sawatzki, Victor-Felix Mautner, David N Cooper
Journal of Medical Genetics
|
February 12, 2013
From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic disease
Chee-Seng Ku, Eng King Tan, David N Cooper
Expert Review of Molecular Diagnostics
|
May 24, 2012
The 'sequence everything' approach and personalized clinical decision challenges
Chee-Seng Ku, David N Cooper, Dimitrios H Roukos
Human Genomics
|
September 5, 2015
Trans-species polymorphism in humans and the great apes is generally maintained by balancing selection that modulates the host immune response
Luisa Azevedo, Catarina Serrano, Antonio Amorim, et al.
Methods in Molecular Medicine
|
January 22, 2004
Neurofibromatosis type 1: a common familial cancer syndrome
Meena Upadhyaya, Peter Thompson, Song Han, et al.
Current Protocols in Bioinformatics
|
April 23, 2008
The Human Gene Mutation Database (HGMD) and its exploitation in the study of mutational mechanisms
David N Cooper, Peter D Stenson, Nadia A Chuzhanova
World Journal of Gastroenterology
|
April 20, 2013
Clinical relevance of cancer genome sequencing
Chee Seng Ku, David N Cooper, Dimitrios H Roukos
Page
of 40