Clinical and genetic characteristics of type 3 lissencephaly caused by a mutation in the TUBA1A gene (OMIM: 611603) by D. M. Guseva, T. V. Markova, L. A. Bessonova, S. S. Nikitin, E. L. Dadali, O. A. Shchagina

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Special clinical manifestations and genetic characteristics of schaaf–Yang syndrome in Russian patients by E. L. Dadali, T. V. Markova, F. M. Bostanova, A. S. Kuchina, L. A. Bessonova, E. A. Melnik, V. V. Zabnenkova, O. P. Ryzhkova, O. E. Agranovich

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Phenotypic variability in TRPV4-associated neuropathies and neuronopathies: a case series by A. F. Murtazina, P. N. Tsabay, G. E. Rudenskaya, L. A. Bessonova, F. M. Bostanova, D. M. Guseva, I. V. Sharkova, O. A. Shchagina, A. A. Orlova, O. P. Ryzhkova, T. V. Markova, A. S. Kuchina, S. S. Nikitin, E. L. Dadali

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