Novel RUNX1 mutations in familial platelet disorder with enh…
Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia%2525253A clues for improved identification of the FPD%2525252FAML syndrome.
Article, Chapter
Full text availability for this item
Journal:
LeukemiaOpens in new Window
Collection:
Springer Complete Journals
Coverage:
- 1997-01-01~present