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Cytogenetic and Genome Research|March 17, 2009
CNV and nervous system diseases--what's new?W Gu, J R LupskiCytogenetic and Genome Research|March 17, 2009
Copy number variations in chronic pancreatitisJ M Chen, E Masson, C Le Maréchal, et al.Cytogenetic and Genome Research|March 17, 2009
The emerging role of structural variations in common disorders: initial findings and discovery challengesL Armengol, R Rabionet, X EstivillCytogenetic and Genome Research|March 17, 2009
Copy number variation of Fc gamma receptor genes and disease predispositionM Fanciulli, T J Vyse, T J AitmanCytogenetic and Genome Research|March 17, 2009
Chromosome copy number variation and breast cancer riskS Tchatchou, B BurwinkelCytogenetic and Genome Research|March 17, 2009
CNVs of human genes and their implication in pharmacogeneticsI Johansson, M Ingelman-SundbergCytogenetic and Genome Research|March 17, 2009
Genomic drift and copy number variation of chemosensory receptor genes in humans and miceM Nozawa, M NeiCytogenetic and Genome Research|March 17, 2009
The evolutionary significance of copy number variation in the human genomeG H PerryCytogenetic and Genome Research|March 17, 2009
Methods to detect CNVs in the human genomeE Aten, S J White, M E Kalf, et al.Cytogenetic and Genome Research|March 17, 2009
Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assaysL Winchester, D F Newbury, A P Monaco, et al.Pageof 263