Associated Papers
The landscape of rare genetic variants in familial Waldenström macroglobulinemia.
Pemov A et al.
Blood Neoplasia, 2024
39036705 (PubMed )
Supplement: BNEO_NEO-2023-000111-mmc8.xlsx › Supplementary_Table_7C
Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients.
Gorski MM et al.
Blood, 2016
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