Associated Papers
Mutational Profile Enables the Identification of a High-Risk Subgroup in Myelodysplastic Syndromes with Isolated Trisomy 8.
Toribio-Castelló S et al.
Cancers, 2023
37568638 (PubMed )
Supplement: cancers-15-03822-s001.zip › Supplementary_tables.xlsx › Table_S2
Triple-Negative Essential Thrombocythemia: Clinical-Pathological and Molecular Features. A Single-Center Cohort Study.
Cattaneo D et al.
Frontiers in Oncology, 2021
33791220 (PubMed )
Supplement: Data_Sheet_1.pdf
Molecular characterization of secretor type alpha(1, 2)-fucosyltransferase gene deficiency in the Philippine population.
Peng CT et al.
Annals of Hematology, 1999
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