High-performance sequencing in the diagnosis of monogenic diseases: Possibilities and limitations

Por L. I. Shagam, V. Yu. Voinova
Publicado em 2016-04-01

New genome editing technologies in the treatment of X-linked adrenoleukodystrophy

Por V. Yu. Voinova, M. А. Shkolnikova, E. A. Nikolaeva
Publicado em 2020-05-01

Rett syndrome in Russia and abroad: a scientific historical review

Por S. G. Vorsanova, Yu. B. Yurov, V. Yu. Voinova, I. Yu. Yurov
Publicado em 2020-07-01

An algorithm for the diagnosis of X-linked intellectual disability in children

Por V. Yu. Voinova, S. G. Vorsanova, Yu. B. Yurov, I. Yu. Yurov
Publicado em 2016-11-01

High-performance DNA sequencing to identify genetically determined diseases in pediatric practice

Por V. Yu. Voinova, E. A. Nikolaeva, N. V. Shсherbakova, M. I. Yuablonskaya
Publicado em 2019-03-01

Phenotypic variability and modifier variants in children with hereditary heart diseases

Por N. V. Shcherbakova, A. B. Zhironkina, V. Yu. Voinova, R. A. Ildarova, M. A. Shkolnikova
Publicado em 2021-07-01

INTEGRATED CLINICAL AND GENETIC APPROACH FOR DIAGNOSIS OF RETT SYNDROME IN CHILDREN

Por I.Yu. Yurov, S.G. Vorsanova, V.Yu. Voinova- Ulas, P.V. Novikov, Yu.B. Yurov
Publicado em 2007-07-01

Beals syndrome (congenital contractural arachnodactyly) in children: Clinical symptoms, diagnosis, treatment, and prevention

Por A. N. Semyachkina, E. A. Bliznets, V. Yu. Voinova, S. V. Bochenkov, M. N. Kharabadze, E. A. Nikolaeva, A. V. Polyakov
Publicado em 2016-11-01

Biomarkers of early cardiovascular aging

Por O. S. Groznova, I. M. Miklashevich, V. Yu. Voinova, M. A. Shkolnikova, O. N. Tkacheva, E. N. Dudinskaya, I. A. Kovalev
Publicado em 2019-09-01