Phenotype in a patient with p.D50N mutation in GJB2 gene resemble both KID and Clouston syndromes von Markova, T.G, Brazhkina, N.B, Bliznech, E.A, Bakhshinyan, V.V, Polyakov, A.V, Tavartkiladze, G.A

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Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population von 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.

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Cochlear outer hair cell bending in an external electric field von Frolenkov, G.I., Kalinec, F., Tavartkiladze, G.A., Kachar, B.

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Electrophysiological measures of cochlear function in guinea pigs with long-term endolymphatic hydrops von Harrison, R.V., Gottesberge, A.Orsulakova-Meyer zum, Erre, J.-P., Mori, N., Aran, J.-M., Morgenstern, C., Tavartkiladze, G.A.

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