Associated Papers
Whole Exome Sequencing of Intermediate-Risk Acute Myeloid Leukemia without Recurrent Genetic Abnormalities Offers Deeper Insights into New Diagnostic Classifications.
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International Journal of Molecular Sciences, 2024
39201354 (PubMed )
Supplement: ijms-25-08669-s001.zip › ijms-3087068-supplementary › Supplementary_Tables_S1-S5.xlsx › Table_S1
ASXL1 mutations predict inferior molecular response to nilotinib treatment in chronic myeloid leukemia.
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Leukemia, 2022
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Supplement: 41375_2022_1648_MOESM1_ESM.xlsx › Genomic_data
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