Showing 1 - 13 results of 13 for search 'A. Kashevarova', query time: 0.03s
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Non-fungible token: a promising digital tool for business by N. A. Kashevarova, I. S. Starikova
Published 2022-05-01
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Analysis of the use of the electronic document management system in federal executive authorities by N. A. Ivanov, N. A. Kashevarova
Published 2021-09-01
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CONCEPTUAL MODEL OF AN IT-SOLUTIONS FOR PATENT RESEARCH AUTOMATION by N. A. Kashevarova, V. O. Gorogankin, P. A. Slobodyansky
Published 2020-07-01
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Generation of the induced pluripotent stem cell line, ICAGi002-A, from unaffected carrier megabase scaled duplication involving the CNTN6 gene by M.M. Gridina, T.V. Nikitina, I.E. Pristyazhnyuk, A.A. Kashevarova, M.E. Lopatkina, S.A. Vasilyev, L.P. Nazarenko, I.N. Lebedev, O.L. Serov
Published 2019-10-01
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46,XY,r(8)/45,XY,−8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study by Anna A. Kashevarova, Tatyana V. Nikitina, Larisa I. Mikhailik, Elena O. Belyaeva, Stanislav A. Vasilyev, Mariya E. Lopatkina, Dmitry A. Fedotov, Elizaveta A. Fonova, Aleksei A. Zarubin, Aleksei A. Sivtsev, Nikolay A. Skryabin, Lyudmila P. Nazarenko, Igor N. Lebedev
Published 2020-12-01
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Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies by E. A. Fonova, A. A. Kashevarova, M. E. Lopatkina, A. A. Sivtsev, A. A. Zarubin, V. V. Demeneva, G. N. Seitova, L. I. Minaycheva, O. A. Salyukova, S. V. Fadyushina, V. V. Petrova, E. O. Belyaeva, L. P. Nazarenko, I. N. Lebedev
Published 2023-03-01
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Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing by Igor N. Lebedev, Tatyana V. Karamysheva, Eugeny A. Elisaphenko, Alexey I. Makunin, Daria I. Zhigalina, Maria E. Lopatkina, Gleb V. Drozdov, Aleksander D. Cheremnykh, Natalia B. Torkhova, Gulnara N. Seitova, Stanislav A. Vasilyev, Anna A. Kashevarova, Ludmila P. Nazarenko, Nikolay B. Rubtsov
Published 2021-08-01
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Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability by A. A. Kashevarova, E. O. Belyaeva, E. A. Fonova, M. E. Lopatkina, O. Y. Vasilyeva, D. A. Fedotov, A. A. Zarubin, A. A. Sivtsev, V. V. Demeneva, O. A. Salyukova, V. V. Petrova, S. V. Fadiushina, L. I. Minaycheva, G. N. Seitova, L. P. Nazarenko, I. N. Lebedev
Published 2023-03-01
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A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication by T. V. Karamysheva, T. V. Karamysheva, I. N. Lebedev, I. N. Lebedev, L. I. Minaycheva, L. P. Nazarenko, L. P. Nazarenko, A. A. Kashevarova, D. A. Fedotov, N. A. Skryabin, M. E. Lopatkina, A. D. Cheremnykh, E. A. Fonova, E. A. Fonova, T. V. Nikitina, E. A. Sazhenova, M. M. Skleimova, N. A. Kolesnikov, G. V. Drozdov, Y. S. Yakovleva, Y. S. Yakovleva, G. N. Seitova, K. E. Orishchenko, K. E. Orishchenko, N. B. Rubtsov, N. B. Rubtsov
Published 2024-03-01
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