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Vol 23, No 3 (2024)
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
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.
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(Rus)
Vol 17, No 4 (2018)
The case of rare hereditary thrombocytopenia with a predisposition to the development of acute myeloid leukemia in twin children
Khajieva F.R., Zharkov P.A., Fedorova D.V., Raykina E.V., Ignatova A.A., Plyasunova S.A., Panteleev M.A.
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(Rus)
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