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Autor:
Albitar F, Kevin Diep, S. Agersborg, Wanlong Ma, De Dios I, Maher Albitar, S. Brodie, M. Thangavelu
Publikováno v:
Genetic Testing and Molecular Biomarkers. 20:341-345
Demonstrating the presence of myelodysplastic syndrome (MDS)-specific molecular abnormalities can aid in diagnosis and patient management. We explored the potential of using peripheral blood (PB) cell-free DNA (cf-DNA) and next-generation sequencing