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Article

Correlations of JAK2–V617F mutation with clinical and laboratory findings in patients with myeloproliferative disorders

15 Oct 2006

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 17045648
DOI: 10.1016/j.leukres.2006.09.005

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Related research

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Correlations of JAK2–V617F mutation with clinical and laboratory findings in patients with myeloproliferative disordersPMID 17045648Read ↗

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JAK2 V617F Mutational Burden and Clinical Findings Relationship in Myeloproliferative NeoplasmsSemantic proximity Read ↗

A JAK2 mutation in myeloproliferative disorders: pathogenesis and therapeutic and scientific prospectsSemantic proximity Read ↗

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JAK2 V617F: a single mutation in the myeloproliferative group of disorders.Semantic proximity Read ↗

JAK2: implications for diagnosis and classification of myeloproliferative disorders.Semantic proximity Read ↗

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Myeloproliferative neoplasms and JAK2 mutations.Semantic proximity Read ↗

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Clinical implications of JAK2 mutations in myeloproliferative disorders.Semantic proximity Read ↗

[Myeloproliferative diseases caused by Jak2 gene mutation].Semantic proximity Read ↗

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