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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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| Huvudupphovsmän: | , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2012
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| Ämnen: | |
| Länkar: | 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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