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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Detalles Bibliográficos
Autores principales: Canales, Cesar P, Walz, Katherina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2011
Materias:
Closeup
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401997/
https://www.ncbi.nlm.nih.gov/pubmed/21204264
http://dx.doi.org/10.1002/emmm.201000111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401997/
https://www.ncbi.nlm.nih.gov/pubmed/21204264
http://dx.doi.org/10.1002/emmm.201000111

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