Search Results - "Tomsky, M. I."

Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A by Solovyev, A. V., Barashkov, N. A., Teryutin, F. M., Pshennikova, V. G., Romanov, G. P., Rafailov, A. M., Sazonov, N. N., Dzhemileva, L. U., Tomsky, M. I., Posukh, O. L., Khusnutdinova, E. K., Fedorova, S. A.

“…We present the results of analysis of skin epidermis thickness in individuals with recessive mutation c.-23+1G>A in the GJB2 gene in comparison with…”
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X-RAY DENSITOMETRY AND FRAX MODEL IN PREDICTING THE RISK OF OSTEOPOROSIS AND LOW-ENERGY FRACTURES IN POSTMENOPAUSAL WOMEN by Epanov, V V, Palshin, G A, Epanova, A A, Komissarov, A N, Tomsky, M I, Sedunov, V F, Egorov, P L

“…88 people of 50 years of age and older were put in this cross-sectional study. The main risk factors for osteoporosis and bone fractures were obtained using…”
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Analysis of GJB6 (Сx30) and GJB3 (Сx31) genes in deaf patients with monoallelic mutations in GJB2 (Сx26) gene in the Sakha Republic (Yakutia) by Pshennikova, V. G., Barashkov, N. A., Solovyev, A. V., Romanov, G. P., Diakonov, E. E., Sazonov, N. N., Morozov, I. V., Bondar, A. A., Posukh, O. L., Dzhemileva, L. U., Khusnutdinova, E. K., Tomsky, M. I., Fedorova, S. A.

“…Тhe DNA testing of autosomal recessive deafness type 1A (DFNB1A, MIM 220290) is complicated when deaf patients have only monoallelic (heterozygous) recessive…”
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Marital Structure, Genetic Fitness, and the GJB2 Gene Mutations among Deaf People in Yakutia (Eastern Siberia, Russia) by Romanov, G. P., Barashkov, N. A., Teryutin, F. M., Lashin, S. A., Solovyev, A. V., Pshennikova, V. G., Bondar, A. A., Morozov, I. V., Sazonov, N. N., Tomsky, M. I., Dzhemileva, L. U., Khusnutdinova, E. K., Posukh, O. L., Fedorova, S. A.

“…Autosomal recessive deafness type 1A (DFNB1A) caused by mutations in the GJB2 gene (Cx26) is the main cause of nonsyndromic hearing impairment in many…”
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