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Annals of Neurology
|
January 26, 2012
Exome sequencing: dual role as a discovery and diagnostic tool
Chee-Seng Ku, David N Cooper, Constantin Polychronakos, et al.
Journal of Human Genetics
|
December 2, 2011
Regions of homozygosity in three Southeast Asian populations
Shu-Mei Teo, Chee-Seng Ku, Agus Salim, et al.
Journal of Human Genetics
|
June 3, 2011
A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals
Shu-Mei Teo, Chee-Seng Ku, Nasheen Naidoo, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
April 24, 2012
Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X
Chee-Seng Ku, David N Cooper, Mengchu Wu, et al.
Expert Review of Molecular Diagnostics
|
April 4, 2012
Exome versus transcriptome sequencing in identifying coding region variants
Chee-Seng Ku, Mengchu Wu, David N Cooper, et al.
Expert Review of Molecular Diagnostics
|
February 29, 2012
Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis
Chee-Seng Ku, Mengchu Wu, David N Cooper, et al.
Journal of Human Genetics
|
June 17, 2011
Copy number polymorphisms in new HapMap III and Singapore populations
Chee-Seng Ku, Shu-Mei Teo, Nasheen Naidoo, et al.
Human Mutation
|
May 28, 2010
Genomic copy number variations in three Southeast Asian populations
Chee-Seng Ku, Yudi Pawitan, Xueling Sim, et al.
Genome Research
|
August 25, 2009
Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations
Yik-Ying Teo, Xueling Sim, Rick T H Ong, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
Annals of Neurology
|
January 26, 2012
Exome sequencing: dual role as a discovery and diagnostic tool
Chee-Seng Ku, David N Cooper, Constantin Polychronakos, et al.
Journal of Human Genetics
|
December 2, 2011
Regions of homozygosity in three Southeast Asian populations
Shu-Mei Teo, Chee-Seng Ku, Agus Salim, et al.
Journal of Human Genetics
|
June 3, 2011
A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals
Shu-Mei Teo, Chee-Seng Ku, Nasheen Naidoo, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
April 24, 2012
Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X
Chee-Seng Ku, David N Cooper, Mengchu Wu, et al.
Expert Review of Molecular Diagnostics
|
April 4, 2012
Exome versus transcriptome sequencing in identifying coding region variants
Chee-Seng Ku, Mengchu Wu, David N Cooper, et al.
Expert Review of Molecular Diagnostics
|
February 29, 2012
Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis
Chee-Seng Ku, Mengchu Wu, David N Cooper, et al.
Journal of Human Genetics
|
June 17, 2011
Copy number polymorphisms in new HapMap III and Singapore populations
Chee-Seng Ku, Shu-Mei Teo, Nasheen Naidoo, et al.
Human Mutation
|
May 28, 2010
Genomic copy number variations in three Southeast Asian populations
Chee-Seng Ku, Yudi Pawitan, Xueling Sim, et al.
Genome Research
|
August 25, 2009
Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations
Yik-Ying Teo, Xueling Sim, Rick T H Ong, et al.
Page
of 3