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Genome Architecture and Its Roles in Human Copy Number Variation
Besides single-nucleotide variants in the human genome, large-scale genomic variants, such as copy number variations (CNVs), are being increasingly discovered as a genetic source of human diversity and the pathogenic factors of diseases. Recent experimental findings have shed light on the links betw...
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| Publicado no: | Genomics Inform |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korea Genome Organization
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4330246/ https://ncbi.nlm.nih.gov/pubmed/25705150 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5808/GI.2014.12.4.136 |
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