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Title
Authors
No 10 (2019)
A study of polymorphisms rs3020434, rs11742635, rs124577644, rs12637801, rs2861221, and rs17677069 in women with uterine leiomyomas and a family history of the disease
Sogoyan N.S., Kuznetsova M.V., Lolomadze E.A., Mikhailovskaya G.V., Mishina N.D., Trofimov D.Y., Adamyan L.V.
PDF
(Rus)
No 12 (2021)
The breast and sex hormones
Smetnik A.A., Rodionov V.V., Kometova V.V., Burmenskaya O.V., Dardyk M.V., Sencha A.N., Ermakova E.I., Ashrafyan L.A.
PDF
(Rus)
No 12 (2018)
Somatic mutations in MED 12 gene exon 2 in women with a single uterine fibroid or multiple ones
Sogoyan N.S., Kuznetsova M.V., Asaturova A.V., Adamyan L.V., Trofimov D.Y.
PDF
(Rus)
No 4-1 (2012)
USE OF PREIMPLANTATION DIAGNOSIS WITHIN THE FRAMEWORK OF AN ASSISTED REPRODUCTIVE TECHNOLOGY PROGRAM FOR MARRIED COUPLES WITH A COMBINATION OF MUTATIONS AT THE AZF LOCUS OF THE Y CHROMOSOME AND CFTR GENE POLYMORPHISM IN HUSBANDS
BELYAEVA N.A., GLINKINA Z.I., SOKUR S.A., GUBAYEVA Z.M., DOLGUSHINA N.V., KALININIA E.A.
PDF
(Rus)
No 1 (2022)
The significance of the oocyte factor in the development of infertility of unclear genesis
Kirakosyan E.V., Ekimov A.N., Pavlovich S.V.
PDF
(Rus)
No 1S (2020): Supplement
Prophylactic surgery in carriers of BRCA1 or BRCA2 gene mutation
Gorodnova T.V., Sokolenko A.P., Kotiv K.B., Yakovleva M.G., Lavrinovich O.E., Mikaya N.A., Ibragimov Z.N., Trifanov Y.N., Bondarev N.E., Nekrasova E.A., Sidoruk A.A., Smirnova O.A., Guseinov K.D., Bakhidze E.V., Meshkova I.E., Bakaeva E.K., Shikhzadaeva M.G., Ul’rikh E.A., Urmancheeva A.F., Berlev I.V., Imyanitov E.N., Belyaev A.M.
PDF
(Rus)
No 7 (2013)
ROLE OF HEREDITARY THROMBOPHILIA IN THE GENESIS OF COMPLICATED PREGNANCY
ZARUDSKAYA O.M., CHURNOSOV M.I.
PDF
(Rus)
1 - 7 of 7 Items

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