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Genome-wide sequencing to identify the cause of hereditary cancer syndromes: with examples from familial pancreatic cancer
Advances in our understanding of the human genome and next-generation technologies have facilitated the use of genome-wide sequencing to decipher the genetic basis of Mendelian disease and hereditary cancer syndromes. The application of genome-wide sequencing in hereditary cancer syndromes has had m...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3652916/ https://ncbi.nlm.nih.gov/pubmed/23196058 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.canlet.2012.11.008 |
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