Showing 1 - 5 results of 5 for search 'D.A. Fedotov', query time: 0.03s Refine Results
  1. 1
    METHOD FOR DETERMINING OF SOUNDS LOCALIZATION IN THREEDIMENSIONAL SPACE FOR DIAGNOSIS OF PNEUMONIA IN YOUNG

    METHOD FOR DETERMINING OF SOUNDS LOCALIZATION IN THREEDIMENSIONAL SPACE FOR DIAGNOSIS OF PNEUMONIA IN YOUNG by A. E. Apikova, D. A. Fedotov, V. A. Klymenko

    Published 2015-05-01
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  2. 2
    A subgroup of light-driven sodium pumps with an additional Schiff base counterion

    A subgroup of light-driven sodium pumps with an additional Schiff base counterion by E. Podoliak, G. H. U. Lamm, E. Marin, A. V. Schellbach, D. A. Fedotov, A. Stetsenko, M. Asido, N. Maliar, G. Bourenkov, T. Balandin, C. Baeken, R. Astashkin, T. R. Schneider, A. Bateman, J. Wachtveitl, I. Schapiro, V. Busskamp, A. Guskov, V. Gordeliy, A. Alekseev, K. Kovalev

    Published 2024-04-01
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  3. 3
    Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability

    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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  4. 4
    Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single‐Gene BDH1 Duplications

    Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single‐Gene BDH1... by A. A. Kashevarova, M. E. Lopatkina, O. Yu. Vasilyeva, D. A. Fedotov, A. D. Lobanov, E. A. Fonova, I. Z. Zhalsanova, A. A. Zarubin, O. A. Salyukova, E. O. Belyaeva, V. V. Petrova, E. G. Ravzhaeva, A. A. Agafonova, A. D. Cheremnykh, N. B. Torkhova, S. L. Vovk, I. N. Lebedev

    Published 2025-01-01
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  5. 5
    A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication

    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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