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Article

JAK2V617F mutation in a 9-year-old girl with polycythemia vera and Budd-Chiari syndrome: a case report.

Journal of pediatric hematology/oncology - 1 Apr 2012

Benedik-Dolničar Majda, Homan Matjaz, Brecelj Jernej

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Identifiers

PMID: 21552144
DOI: 10.1097/MPH.0b013e31820150bf

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JAK2V617F mutation in a 9-year-old girl with polycythemia vera and Budd-Chiari syndrome: a case report.PMID 21552144Read ↗

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A Clue in JAK2: Masked Polycythemia Vera.Semantic proximity Read ↗

Existence of JAK2 mutation 19 years prior to the development of overt polycythemia vera.Semantic proximity Read ↗

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Familial polycythemia vera with non-germline JAK2(V617F) mutation sparing the abnormal and clonal granulopoiesis.Semantic proximity Read ↗

The JAK2V617F mutation is acquired secondary to the predisposing alteration in familial polycythaemia veraSemantic proximity Read ↗

[Polycythemia vera and JAK-2 mutation in childhood: a case report].Semantic proximity Read ↗

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