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Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.
Xavier Estivill and Lluís Armengol
PLoS Genetics 3 (10), e190-1799 (01 Oct 2007)
info:pmid/17953491 | info:doi/10.1371/journal.pgen.0030190
Posted by markcorrales and 5 others to Best genetics review CNV on Tue Nov 27 2007 at 22:13 UTC | info | related
 
Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
Copy number variants and common disorders filling the gaps and exploring complexity in genomewide association studies
Xavier Estivill and Lluís Armengol
PLoS Genetics 3 (10), e190 (01 Oct 2007)
info:doi/10.1371/journal.pgen.0030190
Posted by jbowes and 5 others to copy number on Mon Nov 05 2007 at 11:22 UTC | info | related
 
Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
Copy number variants and common disorders filling the gaps and exploring complexity in genomewide association studies
Xavier Estivill and Lluís Armengol
PLoS Genetics 3 (10), e190 (2007)
info:doi/10.1371/journal.pgen.0030190
Posted by meisel and 5 others to human disease Copy number variation on Wed Oct 31 2007 at 17:43 UTC | info | related
 
Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
Copy number variants and common disorders filling the gaps and exploring complexity in genomewide association studies
PLoS Genetics 3 (10), e190 (2007)
info:doi/10.1371/journal.pgen.0030190
Posted by lindenb and 5 others to genomics genetics toread tutorial review variation Number copy CNV on Fri Oct 26 2007 at 21:18 UTC | info | related
 
Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
Copy number variants and common disorders filling the gaps and exploring complexity in genomewide association studies
Xavier Estivill and Lluís Armengol
PLoS Genetics 3 (10), e190 (01 Oct 2007)
info:doi/10.1371/journal.pgen.0030190
Posted by amybouck and 5 others to CNV on Mon Oct 22 2007 at 02:49 UTC | info | related
 
Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
Copy number variants and common disorders filling the gaps and exploring complexity in genomewide association studies
Xavier Estivill and Lluís Armengol
PLoS Genetics 3 (10), e190 (01 Oct 2007)
info:doi/10.1371/journal.pgen.0030190
Posted by pedrobeltrao and 5 others to review Disease copy-number Polymorphisms on Fri Oct 19 2007 at 11:51 UTC | info | related

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