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Genetic Architecture of Reciprocal CNVs

Copy number variants (CNVs) represent a frequent type of lesion in human genetic disorders that typically affects numerous genes simultaneously. This has raised the challenge of understanding which genes within a CNV drive clinical phenotypes. Although CNVs can arise by multiple mechanisms, a subset...

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Autores principales: Golzio, Christelle, Katsanis, Nicholas
Formato: Artigo
Lenguaje:Inglês
Publicado: 2013
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3740179/
https://ncbi.nlm.nih.gov/pubmed/23747035
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gde.2013.04.013
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