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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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Detalhes bibliográficos
Main Authors: Canales, Cesar P, Walz, Katherina
Formato: Artigo
Idioma:Inglês
Publicado em: WILEY-VCH Verlag 2011
Assuntos:
Acesso em linha: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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