Novel GLIS3 mutation in patient with neonatal diabetes mellitus and congenital hypothyroidism (NDH-syndrome) by Yu. V. Tikhonovich, L. G. Chernich, I. N. Velikanov, V. M. Polyakova, E. V. Vasilyev, V. M. Petrov, E. V. Shreder, Е. V. Glavatskich, A. N. Tyulpakov

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CDC73 mutations in young patients with primary hyperparathyroidism: A description of two clinical cases by E O Mamedova, N G Mokrysheva, E A Pigarova, E G Przhiyalkovskaya, I A Voronkova, E V Vasilyev, V M Petrov, V A Gorbunova, L Ya Rozhinskaya, Zh E Belaya, A N Tyulpakov

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Clinical, hormonal and molecular-genetic characteristics of monogenic diabetes mellitus associated with the mutations in the <i>INS</i> gene by Yu. V. Tikhonovich, E. E. Petryaykina, A. V. Timofeev, N. A. Zubkova, A. A. Kolodkina, E. L. Sorkina, E. V. Vasiliev, V. M. Petrov, E. A. Andrianova, L. I. Zilberman, G. N. Svetlova, A. L. Кalinin, P. M. Rubtsov, S. L. Кiselev, A. V. Panova, E. V. Shreder, T. S. Krasnova, B. P. Kulieva, I. V. Gariaeva, I. G. Rybkina, O. A. Malievskiy, A. N. Tyulpakov

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