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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...
| Formato: | Online Artículo Texto |
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| Lenguaje: | English |
| Publicado: |
Editorial office of Chinese Journal of Hematology
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342541/ https://www.ncbi.nlm.nih.gov/pubmed/30929389 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.03.010 |