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Langerhans cell histiocytosis as a clonal disease of mononuclear phagocyte system
Khynku E.F., Monaenkova M.K., Tamrazova O.B., Taganov A.V., Gureeva М.А., Bagramova G.E., Molochkov A.V.
Genetic predictors of insulin-producing pancreatic tumor
Yukina M.Y., Nuralieva N.F., Troshina E.A.
MUTATIONS OF THE SMARCB1 GENE IN HUMAN CANCERS
Mikhaylenko D.S., Teleshova M.V., Efremov G.D., Alekseev B.Y.
INTERFAMILIAL POLYMORPHISM OF TYPE 1 DYSTONIA
Ostapchuk K.A., Kotov S.V., Sidorova O.P., Polyakov A.V., Galeeva N.M., Misikov V.K.
A clinical case of partial androgen resistance syndrome (Reifenstein syndrome)
Dzeranova L.K., Pigarova E.A., Ivannikova E.V., Kurilo L.F., Chernykh V.B., Polyakov A.V.
Mutations in the HNF1A gene as a cause of MODY3: a clinical case
Demidova T.Y., Gritskevich E.Y., Balutina O.V.
Results of immunohistochemistry diagnostics of breast cancer in the region of Grodno with consideration of the BRCA1 gene mutation in triple negative cancer
Krylov A.Y., Zubritsky M.G., Kurstak I.A., Lialikau S.A., Basinski V.A.
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