Associated Papers
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41422096 (PubMed )
Supplement: 40478_2025_2164_MOESM1_ESM.xlsx › Feuil1
Frequency and clinical impact of WT1 mutations in the context of CEBPA-mutated acute myeloid leukemia.
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Correlation of genetic alterations by whole-exome sequencing with clinical outcomes of glioblastoma patients from the Lebanese population.
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Supplement: pone.0242793.s003.xlsx › Sheet1
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