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A Lower Frequency of Spliceosome Mutations Distinguishes Clonal Cytopenias of Undetermined Significance From Low-Risk Myelodysplastic Syndromes, Despite Inherent Similarities in Genomic, Laboratory, and Clinical Features.
Ferrone, Christina K; McNaughton, Amy J M; Rashedi, Iran; Ring, Brooke; Buckstein, Rena; Tsui, Hubert; Rauh, Michael J.
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  • Ferrone CK; Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada.
  • McNaughton AJM; Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada.
  • Rashedi I; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine and Molecular Diagnostics, Precision Diagnostics and Therapeutics Program, Sunnybrook Health Sciences Centre and Sunnybrook Research Institute, Toronto, Ontario, Can
  • Ring B; Department Medicine, Queen's University, Kingston, Ontario, Canada.
  • Buckstein R; Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Division of Medical Oncology and Hematology, Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada; Odette Cancer Research Program, Sunnybrook Research Institute, Toronto, Ontario, Canada.
  • Tsui H; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine and Molecular Diagnostics, Precision Diagnostics and Therapeutics Program, Sunnybrook Health Sciences Centre and Sunnybrook Research Institute, Toronto, Ontario, Can
  • Rauh MJ; Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada. Electronic address: rauhm@queensu.ca.
Mod Pathol ; 36(3): 100068, 2023 03.
Article en En | MEDLINE | ID: mdl-36788103
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Neoplasias Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Mod Pathol Asunto de la revista: PATOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Canadá
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Neoplasias Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Mod Pathol Asunto de la revista: PATOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Canadá