Rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases
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A. Kohlmann | T. Haferlach | S. Schnittger | W. Kern | C. Haferlach | A. Fasan | F. Dicker | C. Eder
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A. Kohlmann | T. Haferlach | S. Schnittger | W. Kern | C. Haferlach | A. Fasan | F. Dicker | C. Eder