Paul Liu
0000-0002-6779-025X
4 papers found
Refreshing results…
Genomic landscape of patients with germline RUNX1 variants and familial platelet disorder with myeloid malignancy
Differential diagnosis of bone marrow failure syndromes guided by machine learning
A RUNX1-FPDMM rhesus macaque model reproduces the human phenotype and predicts challenges to curative gene therapies
RUNX1 and CBFβ-SMMHC transactivate target genes together in abnormal myeloid progenitors for leukemia development
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