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Replication Stress and Mechanisms of CNV Formation

Copy number variants (CNVs) are widely distributed throughout the human genome, where they contribute to genetic variation and phenotypic diversity. De novo CNVs are also a major cause of numerous genetic and developmental disorders. However, unlike many other types of mutations, little is known abo...

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Detalhes bibliográficos
Main Authors: Arlt, Martin F., Wilson, Thomas E., Glover, Thomas W.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3371136/
https://ncbi.nlm.nih.gov/pubmed/22365495
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gde.2012.01.009
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