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家族性血小板疾病并急性髓系白血病倾向一例报告并文献复习
OBJECTIVE: To analyze the clinical features, bone marrow features, and gene mutations of children with familial platelet disorder with predisposition to myeloid leukemia（FPD/AML）caused by a RUNX1 germline mutation as well as their family members. METHODS: The clinical data and gene mutations of a ch...
Uloženo v:
| Vydáno v: | Zhonghua Xue Ye Xue Za Zhi |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Editorial office of Chinese Journal of Hematology
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8120121/ https://ncbi.nlm.nih.gov/pubmed/33979975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.04.007 |
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