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注意:仅列出部分参考文献,下载原文获取全部文献信息。SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value
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Frequent pathway mutations of splicing machinery in myelodysplasia
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Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia
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Diagnosis and classification of myelodysplastic syndrome: International Working Group on Morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts
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MPL515 mutations in myeloproliferative and other myeloid disorders:: a study of 1182 patients
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