Publication | Closed Access
Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1 targets
62
Citations
40
References
2014
Year
Hematological MalignancyBlood PlateletMedicineGeneticsPlatelet Function DefectGenetic EpidemiologyHematologyPathologyMixed-phenotype Acute LeukemiaFamilial Platelet DisorderCandidate Runx1 TargetsCell BiologyMyeloid Neoplasia
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