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Abnormalities of chromosome 1 in myeloproliferative disorders.
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Hematopathologic findings in the myeloproliferative disorders.
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Pulmonary arterial hypertension and myeloproliferative disorders.
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Bone marrow histopathology in the diagnosis of chronic myeloproliferative disorders: a forgotten pearl.
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Combined plateletpheresis and cytotoxic chemotherapy for symptomatic thrombocytosis in myeloproliferative disorders.
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Mutations in GATA1 in both transient myeloproliferative disorder and acute megakaryoblastic leukemia of Down syndrome.
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The diagnostic interface between histology and molecular tests in myeloproliferative disorders.
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The molecular biology of myeloproliferative disorders as revealed by chromosomal abnormalities.
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Issues in the pathology and diagnosis of the chronic myeloproliferative disorders and the myelodysplastic syndromes.
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Enumeration and immunohistochemical characterisation of bone marrow basophils in myeloproliferative disorders using the basophil specific monoclonal antibody 2D7.
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A new family with a germline ANKRD26 mutation and predisposition to myeloid malignancies.
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A novel TRIP11-FLT3 fusion in a patient with a myeloid/lymphoid neoplasm with eosinophilia.
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AKT is a therapeutic target in myeloproliferative neoplasms.
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Classification and diagnosis of myeloproliferative neoplasms: the 2008 World Health Organization criteria and point-of-care diagnostic algorithms.
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Classification of myeloid neoplasms/acute leukemia: Global perspectives and the international consensus classification approach.
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