Associated Papers
Avoidance of related donors in CAEBV with germline immune variants: long-termoutcome of matched unrelated donor HSCT - a case report.
Wang X et al.
Annals of Hematology, 2026
Clinical characterization and genetic analysis of transient abnormal myelopoiesis without the down syndrome phenotype.
Cai J et al.
Molecular Genetics and Metabolism Reports, 2025
Treatment of three pediatric AML co-expressing NUP98-NSD1, FLT3-ITD, and WT1.
Liu L et al.
Bmc Pediatrics, 2024
Identification of rare coding variants in TYK2 protective for rheumatoid arthritis in the Japanese population and their effects on cytokine signalling.
Motegi T et al.
Annals of the Rheumatic Diseases, 2019
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