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Novel RUNX1 mutations in familial platelet disorder with enh…
Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia%3A clues for improved identification of the FPD%2FAML syndrome.
Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia%3A clues for improved identification of the FPD%2FAML syndrome.
Article, Chapter
Authors: M.C.J. Jongmans
Publication: Leukemia, Volume:24, Issue:1, Page(s):242-246
ISSN: 0887-6924
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View Full Text Source:Leukemia,Leukemia,Springer Complete Journals Opens in new Window
Journal:  Leukemia Source:Springer Complete Journals Opens in new Window
Collection:  Springer Complete Journals Opens in new Window
Coverage:
  • 1997-01-01~present; volume:11~present;issue:1~present
View Full Text Source:Leukemia,Leukemia,Nature All Titles Opens in new Window
Journal:  Leukemia Source:Nature All Titles Opens in new Window
Collection:  Nature All Titles Opens in new Window
Coverage:
  • 1997-01~present; volume:11~present;issue:1~present
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