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Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies.
Decker, Melanie; Lammens, Tim; Ferster, Alina; Erlacher, Miriam; Yoshimi, Ayami; Niemeyer, Charlotte M; Ernst, Martijn P T; Raaijmakers, Marc H G P; Duployez, Nicolas; Flaum, Andreas; Steinemann, Doris; Schlegelberger, Brigitte; Illig, Thomas; Ripperger, Tim.
Afiliación
  • Decker M; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
  • Lammens T; Department of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium.
  • Ferster A; Hematology-Oncology, Queen Fabiola Children's University Hospital (ULB), Brussels, Belgium.
  • Erlacher M; Division of Pediatric Hematology-Oncology, Department of Pediatric and Adolescent Medicine, University of Freiburg, Freiburg, Germany.
  • Yoshimi A; Division of Pediatric Hematology-Oncology, Department of Pediatric and Adolescent Medicine, University of Freiburg, Freiburg, Germany.
  • Niemeyer CM; Division of Pediatric Hematology-Oncology, Department of Pediatric and Adolescent Medicine, University of Freiburg, Freiburg, Germany.
  • Ernst MPT; Department of Hematology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Raaijmakers MHGP; Department of Hematology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Duployez N; Department of Hematology, CHU Lille, INSERM, University Lille, Lille, France.
  • Flaum A; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
  • Steinemann D; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
  • Schlegelberger B; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
  • Illig T; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
  • Ripperger T; Hannover Unified Biobank, Hannover Medical School, Hannover, Germany.
Leukemia ; 35(11): 3304-3308, 2021 11.
Article en En | MEDLINE | ID: mdl-33692461
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de las Plaquetas Sanguíneas / Leucemia Mieloide Aguda / Leucemia Eritroblástica Aguda / Subunidad alfa 2 del Factor de Unión al Sitio Principal / Subunidad beta del Factor de Unión al Sitio Principal / Mutación / Trastornos Mieloproliferativos Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Leukemia Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de las Plaquetas Sanguíneas / Leucemia Mieloide Aguda / Leucemia Eritroblástica Aguda / Subunidad alfa 2 del Factor de Unión al Sitio Principal / Subunidad beta del Factor de Unión al Sitio Principal / Mutación / Trastornos Mieloproliferativos Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Leukemia Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido