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骨髓增生异常综合征RAS基因突变的分子学特征及预后意义
OBJECTIVE: To explore the molecular features and prognostic value of RAS mutations in patients with myelodysplastic syndromes(MDS). METHODS: 112-gene targeted sequencing was conducted to detect RAS mutations in 776 patients with newly diagnosed primary MDS from December 2011 to December 2018. The mu...
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| Publicado no: | Zhonghua Xue Ye Xue Za Zhi |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Editorial office of Chinese Journal of Hematology
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7595862/ https://ncbi.nlm.nih.gov/pubmed/33113603 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.09.004 |
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