NPM1 mutation but not RUNX1 mutation or multilineage dysplasia defines a prognostic subgroup within de novo acute myeloid leukemia lacking recurrent cytogenetic abnormalities in the revised 2016 WHO classification

著录项

• 来源
  《American Journal of Hematology》 |2017年第7期|共2页
• 作者

  Weinberg Olga K.; Gibson Christopher J.; Blonquist Traci M.; Neuberg Donna; Pozdnyakova Olga; Kuo Frank; Ebert Benjamin L.; Hasserjian Robert P.;

  展开▼
• 作者单位

  Boston Childrens Hosp Dept Pathol 300 Longwood Ave Bader 126-2 Boston MA 02115 USA;

  Brigham &

  Womens Hosp Div Hematol Dana Farber Canc Inst Boston MA 02115 USA;

  Dana Farber Canc Inst Dept Biostat &

  Computat Biol Boston MA 02115 USA;

  Dana Farber Canc Inst Dept Biostat &

  Computat Biol Boston MA 02115 USA;

  Brigham &

  Womens Hosp Dept Pathol 75 Francis St Amory 3 Boston MA 02115 USA;

  Brigham &

  Womens Hosp Dept Pathol 75 Francis St Amory 3 Boston MA 02115 USA;

  Brigham &

  Womens Hosp Div Hematol Dana Farber Canc Inst Boston MA 02115 USA;

  Massachusetts Gen Hosp Dept Pathol WRN244 55 Fruit St Boston MA 02114 USA;

  展开▼
• 收录信息
• 原文格式 PDF
• 正文语种 eng
• 中图分类 血液及淋巴系疾病;
• 关键词