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The impact of human copy number variation on gene expression

Recent years have witnessed a flurry of important technological and methodological developments in the discovery and analysis of copy number variations (CNVs), which are increasingly enabling the systematic evaluation of their impact on a broad range of phenotypes from molecular-level (intermediate)...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Brief Funct Genomics
Päätekijät: Gamazon, Eric R., Stranger, Barbara E.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2015
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4592354/
https://ncbi.nlm.nih.gov/pubmed/25922366
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bfgp/elv017
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