Open access
Sep 2026
Genomic Characterization of ETV6::RUNX1‐Positive Childhood B‐ALL in a Chinese Cohort: Novel Fusion Partners, Co‐Occurring Mutations, and Risk‐Stratifying Biomarkers
ETV6::RUNX1 is the most common genetic abnormality in pediatric B‐cell acute lymphoblastic leukemia (ALL; ∼25%), yet the comprehensive genetic architecture and molecular predictors of intermediate‐risk (IR) stratification remain incompletely characterized.
Hua-Lei Luo, Gui-Chi Zhou, Qian Li et al.
· Pediatric Blood & Cancer · 0 citations