RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM)
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference70 articles.
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5. Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions;Quentin;Blood,2011
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