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Recurrent DNA inversion rearrangements in the human genome
Several lines of evidence suggest that reiterated sequences in the human genome are targets for nonallelic homologous recombination (NAHR), which facilitates genomic rearrangements. We have used a PCR-based approach to identify breakpoint regions of rearranged structures in the human genome. In part...
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
National Academy of Sciences
2007
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1832218/ https://ncbi.nlm.nih.gov/pubmed/17389356 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0701631104 |
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