Additional genetic aberrations detected by fluorescence in situ hybridization in children with acute lymphoblastic leukemia and the t(12;21)(p13;q22)/ETV6::RUNX1 translocation: an association with initial clinical and laboratory findings and response to therapy - PDF (Russian)


Copyright (c) 2025 Kotov I.S., Tsaur G.A., Nokhrina E.S., Ryakshina A.V., Olshanskaya Y.V., Permikin Z.V., Verzhbitskaya T.Y., Riger T.O., Ponomarev A.I., Streneva O.V., Arakaev O.R., Tsvirenko S.V., Kovtun O.P., Fechina L.G.

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.