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Coincidence of 5q deletion and the JAK2V617F mutation: report of two patients with overlapping myelodysplastic and myeloproliferative features and review of the literature.
Bürki, Susanne; Shumilov, Evgenii; Bonadies, Nicolas; Flach, Johanna; Legros, Myriam; Banz, Yara; Oppliger-Leibundgut, Elisabeth; Fiedler, Martin; Angelillo-Scherrer, Anne; Rovo, Alicia; Bacher, Ulrike.
Afiliação
  • Bürki S; a Department of Haematology , Inselspital, Bern University Hospital, University of Bern , Bern , Switzerland.
  • Shumilov E; b Department of Haematology and Clinical Oncology , University Medicine Göttingen (UMG) , Göttingen , Germany.
  • Bonadies N; a Department of Haematology , Inselspital, Bern University Hospital, University of Bern , Bern , Switzerland.
  • Flach J; b Department of Haematology and Clinical Oncology , University Medicine Göttingen (UMG) , Göttingen , Germany.
  • Legros M; c Institute of Molecular Oncology , University Medicine Göttingen (UMG) , Göttingen , Germany.
  • Banz Y; a Department of Haematology , Inselspital, Bern University Hospital, University of Bern , Bern , Switzerland.
  • Oppliger-Leibundgut E; d Center of Laboratory Medicine (ZLM) , Inselspital, Bern University Hospital, University of Bern , Bern , Switzerland.
  • Fiedler M; e Institute of Pathology , University of Bern , Bern , Switzerland.
  • Angelillo-Scherrer A; a Department of Haematology , Inselspital, Bern University Hospital, University of Bern , Bern , Switzerland.
  • Rovo A; f Department of Clinical Research , University of Bern , Bern , Switzerland.
  • Bacher U; d Center of Laboratory Medicine (ZLM) , Inselspital, Bern University Hospital, University of Bern , Bern , Switzerland.
Leuk Lymphoma ; 59(9): 2233-2237, 2018 09.
Article em En | MEDLINE | ID: mdl-29295644
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 5 / Deleção Cromossômica / Mutação de Sentido Incorreto / Janus Quinase 2 / Doenças Mieloproliferativas-Mielodisplásicas Tipo de estudo: Diagnostic_studies Limite: Aged80 / Female / Humans Idioma: En Revista: Leuk Lymphoma Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Suíça
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 5 / Deleção Cromossômica / Mutação de Sentido Incorreto / Janus Quinase 2 / Doenças Mieloproliferativas-Mielodisplásicas Tipo de estudo: Diagnostic_studies Limite: Aged80 / Female / Humans Idioma: En Revista: Leuk Lymphoma Assunto da revista: HEMATOLOGIA / NEOPLASIAS Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Suíça