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伴TP53基因异常骨髓增生异常综合征患者的临床特征及预后研究
OBJECTIVE: To explore the clinical implications and prognostic value of TP53 gene mutation and deletion in patients with myelodysplastic syndromes (MDS). METHODS: 112-gene targeted sequencing and interphase fluorescence in situ hybridization (FISH) were used to detect TP53 mutation and deletion in 5...
Tallennettuna:
| Julkaisussa: | Zhonghua Xue Ye Xue Za Zhi |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Editorial office of Chinese Journal of Hematology
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7342541/ https://ncbi.nlm.nih.gov/pubmed/30929389 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.03.010 |
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