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CLINICAL EXOME SEQUENCING TO DETECT GENETICALLY DETERMINED DISEASES OF THE SKELETON by I V Kanivets, F A Konovalov, S A Korostelev, N A Belova, F S Katasonov, D V Piankov, D N Khmelkova

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Mutation profile of the tall cell variant of papillary thyroid carcinoma: analysis of 5 cases using wide-panel next-generation sequencing by I. L. Plaksa, M. R. Savchuk, N. V. Shved, N. A. Savelov, D. N. Khmelkova, А. A. Isaev, R. V. Deev

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KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families by G. E. Rudenskaya, V. A. Kadnikova, O. P. Ryzhkova, L. A. Bessonova, E. L. Dadali, D. S. Guseva, T. V. Markova, D. N. Khmelkova, A. V. Polyakov

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