New recurrent large deletion, encompassing both GJB2 and GB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive mode of inheritance
Bliznetz, E. A, Makienko, O. N, Okuneva, E. G, Markova, T. G, Polyakov, A. V
Published in Russian journal of genetics (01.04.2014)
Published in Russian journal of genetics (01.04.2014)
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Spectrum of the GJB2 mutations in Belarussian patients with hearing loss. Findings of pilot genetic screening of hearing impairment in newborns
Bliznetz, E. A, Martsul, D. N, Khorov, O. G, Markova, T. G, Polyakov, A. V
Published in Russian journal of genetics (01.02.2014)
Published in Russian journal of genetics (01.02.2014)
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Journal Article
Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population
Markova, T.G., Alekseeva, N.N., Mironovich, O.L., Galeeva, N.M., Lalayants, M.R., Bliznetz, E.A., Chibisova, S.S., Polyakov, A.V., Tavartkiladze, G.A.
Published in International journal of pediatric otorhinolaryngology (01.11.2020)
Published in International journal of pediatric otorhinolaryngology (01.11.2020)
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Early audiological phenotype in patients with mutations in the USH2A gene
Markova, T.G., Lalayants, M.R., Alekseeva, N.N., Ryzhkova, O.P., Shatokhina, O.L., Galeeva, N.M., Bliznetz, E.A., Weener, M.E., Belov, O.A., Chibisova, S.S., Polyakov, A.V., Tavartkiladze, G.A.
Published in International journal of pediatric otorhinolaryngology (01.06.2022)
Published in International journal of pediatric otorhinolaryngology (01.06.2022)
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Journal Article
CAG polymorphism of the Androgen Receptor gene and semen parameters in pathozoospermic patients with and without Y chromosome microdeletions, and in normozoospermic men
Melikyan, L. P., Bliznetz, E. A., Shtaut, M. I., Sedova, A. O., Sorokina, T. M., Kurilo, L. F., Polyakov, A. V., Chernykh, V. B.
Published in Andrologii͡a︡ i genitalʹnai͡a︡ khirurgii͡a (26.08.2021)
Published in Andrologii͡a︡ i genitalʹnai͡a︡ khirurgii͡a (26.08.2021)
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Journal Article
Twenty years of clinical studies of GJB2-linked hearing loss in Russia
Markova, T G, Bliznetz, E A, Polyakov, A V, Tavartkiladze, G A
Published in Vestnik otorinolaringologii (2018)
Published in Vestnik otorinolaringologii (2018)
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The analysis of the association of the polymorphic variants of the TPMT, COMT, and ABCC3 genes with the development of hearing disorders induced by the cisplatin treatment
Mironovich, O L, Bliznetz, E A, Garbaruk, E S, Belogurova, M B, Subora, N V, Varfolomeeva, S R, Kachanov, D Yu, Shamanskaya, T V, Markova, T G, Polyakov, A V
Published in Vestnik otorinolaringologii (2018)
Published in Vestnik otorinolaringologii (2018)
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The clinical definition and etiology of Pendred syndrome (a review of the literature and clinical observations)
Markova, T G, Geptner, E N, Lalayants, M R, Zelikovich, E I, Chugunova, T I, Mironovich, O L, Bliznetz, E A, Polyakov, A V, Tavartkiladze, G A
Published in Vestnik otorinolaringologii (2016)
Published in Vestnik otorinolaringologii (2016)
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The results of cochlear implantation in the patient with hereditary and non-hereditary hearing loss
Tavartkiladze, G A, Bakhshinyan, V V, Markova, T G, Tsygankova, E R, Petrova, I P, Goykhburg, M V, Chibisova, S S, Bliznetz, E A, Polyakov, A V
Published in Vestnik otorinolaringologii (2016)
Published in Vestnik otorinolaringologii (2016)
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Journal Article
Hidden X Chromosomal Mosaicism in a 46,XX Male
Chernykh, V.B., Kurilo, L.F., Shilova, N.V., Zolotukhina, T.V., Ryzhkova, O.P., Bliznetz, E.A., Polyakov, A.V.
Published in Sexual development (01.01.2009)
Published in Sexual development (01.01.2009)
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Journal Article
DNA copy number analysis of the DFNB1 hereditary hearing loss locus
Bliznetz, E. A., Kanivets, I. V., Polyakov, A. V.
Published in Russian journal of genetics (01.07.2017)
Published in Russian journal of genetics (01.07.2017)
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Journal Article
Polymorphism of CAG Repeats in Exon 1 of the Androgen Receptor Gene in Russian Men with Various Forms of Pathozoospermia
Melikyan, L. P., Bliznetz, E. A., Polyakov, A. V., Mironovich, O. L., Kuznetsova, I. A., Sorokina, T. M., Shtaut, M. I., Sedova, A. O., Kurilo, L. F., Solovova, O. A., Chernykh, V. B.
Published in Russian journal of genetics (01.08.2020)
Published in Russian journal of genetics (01.08.2020)
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Journal Article
Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders
Mironovich, O. L., Bliznetz, E. A., Markova, T. G., Geptner, E. N., Lalayants, M. R., Zelikovich, E. I., Tavartkiladze, G. A., Polyakov, A. V.
Published in Russian journal of genetics (2017)
Published in Russian journal of genetics (2017)
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Journal Article
Changes in the connexin 26 gene (GJB2) in Russian patients with hearing loss: Results of long-term molecular diagnostics of hereditary nonsyndromic hearing loss
Bliznetz, E. A., Galkina, V. A., Matyushchenko, G. N., Kisina, A. G., Markova, T. G., Polyakov, A. V.
Published in Russian journal of genetics (2012)
Published in Russian journal of genetics (2012)
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