Showing 1 - 9 results of 9 for search 'G. N. Seitova', query time: 0.03s
Refine Results
-
1
-
2
-
3
-
4
-
5
-
6
-
7
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
Article -
8
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
Article -
9
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
Article