Novel RUNX1 mutations in familial platelet disorder with enh…
Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia%253A clues for improved identification of the FPD%252FAML syndrome.
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Journal:
LeukemiaOpens in new Window
Collection:
Springer Complete Journals
Opens in new Window
Coverage:
- 1997-01-01~present; volume:11~present;issue:1~present
Journal:
LeukemiaOpens in new Window
Collection:
Nature All Titles
Opens in new Window
Coverage:
- 1997-01~present; volume:11~present;issue:1~present