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Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|July 23, 2003
[DNA-diagnosis of Emery-Dreifuss muscular dystrophy]S M Tverskaia, G E Rudenskaia, A L Chukhrova, et al.Vestnik Oftalmologii|March 15, 2014
[Hereditary optic neuropathies: clinical and molecular genetic characteristics]N A Khanakova, N L Sheremet, A N Loginova, et al.Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|January 18, 2022
[Diversity of CACNA1A-related disorders]G E Rudenskaya, I G Sermyagina, A L Chukhrova, et al.Genetika|July 16, 2008
[Molecular analysis of the Y chromosome in XX sex-reversed patients]V B Chernykh, A L Chukhrova, N N Vasserman, et al.Clinical Genetics|June 20, 2008
Laminopathies in Russian familiesG E Rudenskaya, A V Polyakov, S M Tverskaya, et al.Vestnik Oftalmologii|July 2, 2013
[Clinical and molecular genetic analysis of hereditary optic neuropathies]S É Avetisov, N L Sheremet, O K Vorob'eva, et al.Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|November 23, 2006
[Clinical, genealogical and molecular genetic study of Emery-Dreifuss muscular dystrophy]G E Rudenskaia, S M Tverskaia, A L Chukhrova, et al.American Journal of Medical Genetics. Part A|November 18, 2008
Unique mosaic X/Y translocation/insertion in infant 45,X maleV B Chernykh, S V Vyatkina, V G Antonenko, et al.Vestnik Oftalmologii|May 29, 2014
[Stargardt's disease and abiotrophy of Franceschetti (fundus flavimaculatus): pathogenetic, clinical, and molecular genetic characteristics]M T Bondarenko, N V Zhorzholadze, N L Sheremet, et al.Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|March 5, 2026
[Autosomal dominant dyskinesia associated with the ADCY5 gene]G E Rudenskaya, F M Bostanova, E L Dadaly, et al.Pageof 2