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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Journal Article
Diversity of VCP-related phenotypes: case report and literature review
Rudenskaya, G. E., Mironovich, O. L., Murtazina, A. F., Shchagina, O. A.
Published in Nervno-myshechnye bolezni (19.04.2021)
Published in Nervno-myshechnye bolezni (19.04.2021)
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Journal Article
OTOF-related auditory neuropathy spectrum disorder
Lalayants, M R, Mironovich, O L, Bliznets, E A, Markova, T G, Polyakov, A V, Tavartkiladze, G A
Published in Vestnik otorinolaringologii (2020)
Published in Vestnik otorinolaringologii (2020)
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Journal Article
Diagnostic utility of exome sequencing for inherited peripheral neuropathies
Shchagina, O. A., Ryzhkova, O. P., Chukhrova, A. L., Milovidova, T. V., Gundorova, P., Mironovich, O. L., Orlova, A. A., Orlova, M. D., Poliakov, A. V.
Published in Nervno-myshechnye bolezni (29.12.2020)
Published in Nervno-myshechnye bolezni (29.12.2020)
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Journal Article
Сlinical and Radiological Characteristics of Two Patients with Acromesomelic Dysplasia Maroteaux Type with New Mutation in the NRP2 Gene
Markova, T. V., Kenis, V. M., Mironovich, O. L., Shchagina, O. A., Nagornova, T. S., Melchenko, E. V., Dadali, E. L.
Published in Travmatologii͡a︡ i ortopedii͡a︡ Rossii (01.09.2020)
Published in Travmatologii͡a︡ i ortopedii͡a︡ Rossii (01.09.2020)
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Journal Article
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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Journal Article
Diversity of VCP-related phenotypes: case report and literature review
Rudenskaya, G E, Mironovich, O L, Murtazina, A F, Shchagina, O A
Published in Nervno-myshechnye bolezni (01.01.2021)
Published in Nervno-myshechnye bolezni (01.01.2021)
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Journal Article
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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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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Клинико-генетические характеристики синдрома Бош–Бунстра–Шаафа, обусловленного вновь выявленными мутациями в гене NR2F1
Дадали, Е Л, Боровиков, А О, Щагина, О А, Миронович, О Л, Dadali, E L, Borovikov, A O, Shchagina, O A, Mironovich, O L
Published in Nervno-myshechnye bolezni (01.01.2020)
Published in Nervno-myshechnye bolezni (01.01.2020)
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