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Copy number variation and susceptibility to complex traits

Copy number variations (CNV) within the genome are extremely abundant. In this closeup, Canales and Walz discuss how CNV are associated with normal variation, genomic disorders, genome evolution, adaptive traits and how the use of a novel screen described by Ermakova et al in this issue that is desi...

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Bibliografische gegevens
Hoofdauteurs: Canales, Cesar P, Walz, Katherina
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: WILEY-VCH Verlag 2011
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3401997/
https://ncbi.nlm.nih.gov/pubmed/21204264
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/emmm.201000111
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