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Absence of a common founder mutation in patients with cooccurring myelodysplastic syndrome and plasma cell disorder.
Klimkowska, Monika; Nannya, Yasuhito; Gran, Charlotte; Månsson, Robert; Douagi, Iyadh; Ogawa, Seishi; Nahi, Hareth; Tobiasson, Magnus.
Afiliación
  • Klimkowska M; Department of Clinical Pathology and Cytology, Karolinska University Hospital, Stockholm, Sweden.
  • Nannya Y; Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Gran C; Karolinska University Laboratory, Department of Clinical Chemistry, Stockholm, Sweden.
  • Månsson R; Department of Medicine, Center for Hematology and Regenerative Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Douagi I; Department of Medicine, Center for Hematology and Regenerative Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Ogawa S; Department of Medicine, Center for Hematology and Regenerative Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Nahi H; Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Tobiasson M; Department of Medicine, Center for Hematology and Regenerative Medicine, Karolinska Institutet, Stockholm, Sweden.
Blood ; 137(9): 1260-1263, 2021 03 04.
Article en En | MEDLINE | ID: mdl-33120432
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Plasmáticas / Síndromes Mielodisplásicos / Mutación Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Año: 2021 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Plasmáticas / Síndromes Mielodisplásicos / Mutación Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Año: 2021 Tipo del documento: Article País de afiliación: Suecia Pais de publicación: Estados Unidos