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Chee Seng Ku

Showing results (21-30 of 29) with videos related to

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Annals of Neurology|January 26, 2012
Exome sequencing: dual role as a discovery and diagnostic toolChee-Seng Ku, David N Cooper, Constantin Polychronakos, et al.
Journal of Human Genetics|December 2, 2011
Regions of homozygosity in three Southeast Asian populationsShu-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 individualsShu-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 XChee-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 variantsChee-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 diagnosisChee-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 populationsChee-Seng Ku, Shu-Mei Teo, Nasheen Naidoo, et al.
Human Mutation|May 28, 2010
Genomic copy number variations in three Southeast Asian populationsChee-Seng Ku, Yudi Pawitan, Xueling Sim, et al.
Genome Research|August 25, 2009
Singapore Genome Variation Project: a haplotype map of three Southeast Asian populationsYik-Ying Teo, Xueling Sim, Rick T H Ong, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 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 toolChee-Seng Ku, David N Cooper, Constantin Polychronakos, et al.
Journal of Human Genetics|December 2, 2011
Regions of homozygosity in three Southeast Asian populationsShu-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 individualsShu-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 XChee-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 variantsChee-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 diagnosisChee-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 populationsChee-Seng Ku, Shu-Mei Teo, Nasheen Naidoo, et al.
Human Mutation|May 28, 2010
Genomic copy number variations in three Southeast Asian populationsChee-Seng Ku, Yudi Pawitan, Xueling Sim, et al.
Genome Research|August 25, 2009
Singapore Genome Variation Project: a haplotype map of three Southeast Asian populationsYik-Ying Teo, Xueling Sim, Rick T H Ong, et al.
Pageof 3