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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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| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2013
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| Onderwerpen: | |
| Online toegang: | 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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