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机译:功能获得性JAK2 V617F突变可将原发性血小板增多症和慢性特发性骨髓纤维化的表型转变为更多的“红斑病”和更少的“血栓性红细胞病”:分子,组织学和临床研究
Department of Pathomorphology Collegium Medicum Jagiellonian University Kraków Poland;
Department of Hematology Collegium Medicum Jagiellonian University Kraków Poland;
Department of Pathomorphology Collegium Medicum Jagiellonian University Kraków Poland;
Department of Hematology Collegium Medicum Jagiellonian University Kraków Poland;
Department of Hematology Collegium Medicum Jagiellonian University Kraków Poland;
Department of Hematology Collegium Medicum Jagiellonian University Kraków Poland;
Ludwik Rydygier Memorial District Hospital Kraków Poland;
Ludwik Rydygier Memorial District Hospital Kraków Poland;
Department of Pathomorphology Collegium Medicum Jagiellonian University Kraków Poland;
Department of Pathomorphology Collegium Medicum Jagiellonian University Kraków Poland;
JAK2; Mutation; Myeloproliferative disorders; Trephine bone marrow biopsy;
机译:jak2 jak2 v617f V617f-positive血小板血症和早期原发性骨髓纤维化的比较:突变负担和组织学的影响
机译:无JAK2(V617F)或MPL突变的原发性血小板增多症和原发性骨髓纤维化中国人CALR突变的频率和等位基因负担
机译:在患有原发性血小板增多症和原发性骨髓纤维化的韩国患者中,JAK2 V617F,MPL和CALR突变
机译:在患有原发性血小板增多症和原发性骨髓纤维化的韩国患者中JAK2 V617FMPL和CALR突变
机译:JAK2 V617F在巴西真性红细胞增多症,特发性骨髓纤维化和原发性血小板增多症患者中的患病率