Search Results - M.A. Bolkov

FAMILIAL CASE OF CHROMOSOME 22q11.2 DELETION SYNDROME by I. A. Tuzankina, S. S. Deryabina, E. V. Vlasova, M. A. Bolkov

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TREATMENT OF INFANTS WITH REPEATED BACTERIAL INFECTIONS OF RESPIRATORY TRACT AND ENT-ORGANS WITH LYSATES MIXTURE by E.V. Vlasova, I.A. Tuzankina, V.N. Shershnev, M.A. Bolkov

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Molecular diagnostics of primary immunodeficiencies in Sverdlovsk region by S. S. Deryabina, O. V. Lagutina, I. A. Tuzankina, E. V. Vlasova, M. A. Bolkov

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Oral manifestations of primary immunodeficiencies by M. A. Dolgikh, M. A. Bolkov, I. A. Tuzankina, N. G. Sarkisyan, N. A. Hovsepyan

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Phenotypic manifestation of homozygous partial deletion of the chromosome 1 segment spanning <i>CFHR3</i> region by I. A. Tuzankina, M. A. Bolkov, N. S. Zhuravleva, Yu. O. Vaseneva, Kh. Shinvari, O. V. Schipacheva

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Variability of CATCH-22 symptome complex within the framework of 22q11.2 deletion syndrome by D. A. Cheremokhin, S. S. Deryabina, I. A. Tuzankina, E. V. Vlasova, N. V. Nikitina, M. A. Bolkov

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