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A V Polyakov

Showing results (31-40 of 56) with videos related to

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Heredity|August 1, 1997
Novosibirsk revisited 24 years on: chromosome polymorphism in the Novosibirsk population of the common shrew Sorex araneus LA V Polyakov, N B Chadova, M I Rodionova, et al.
Vestnik Otorinolaringologii|June 2, 2020
[Hearing loss due to mutations or lack of the gene coding protein stereocillin]T G Markova, N N Alekseeva, O L Mironovich, et al.
American Journal of Human Genetics|June 8, 2000
A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light geneI V Mersiyanova, A V Perepelov, A V Polyakov, et al.
Klinicheskaia Laboratornaia Diagnostika|September 12, 2019
[The experience of application of target sequencing in molecular diagnostic of mucoviscidosis.]T S Simakova, A G Bragin, M A Glushkova, et al.
American Journal of Medical Genetics. Part A|November 18, 2008
Unique mosaic X/Y translocation/insertion in infant 45,X maleV B Chernykh, S V Vyatkina, V G Antonenko, et al.
Genetika|January 27, 2018
[Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders]O L Mironovich, E A Bliznetz, T G Markova, et al.
Journal of Biomedical Materials Research. Part A|November 28, 2012
In vitro and in vivo studies on nanocrystalline Ti fabricated by equal channel angular pressing with microcrystalline CP Ti as controlF L Nie, Y F Zheng, S C Wei, et al.
Vestnik Otorinolaringologii|August 17, 2018
[Epidemiology of hearing loss in children of the first year of life]S S Chibisova, T G Markova, N N Alekseeva, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21S M Ismailov, V P Fedotov, E L Dadali, et al.
Vestnik Oftalmologii|October 26, 2022
[Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation)]I V Zolnikova, S V Milash, R A Zinchenko, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Heredity|August 1, 1997
Novosibirsk revisited 24 years on: chromosome polymorphism in the Novosibirsk population of the common shrew Sorex araneus LA V Polyakov, N B Chadova, M I Rodionova, et al.
Vestnik Otorinolaringologii|June 2, 2020
[Hearing loss due to mutations or lack of the gene coding protein stereocillin]T G Markova, N N Alekseeva, O L Mironovich, et al.
American Journal of Human Genetics|June 8, 2000
A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light geneI V Mersiyanova, A V Perepelov, A V Polyakov, et al.
Klinicheskaia Laboratornaia Diagnostika|September 12, 2019
[The experience of application of target sequencing in molecular diagnostic of mucoviscidosis.]T S Simakova, A G Bragin, M A Glushkova, et al.
American Journal of Medical Genetics. Part A|November 18, 2008
Unique mosaic X/Y translocation/insertion in infant 45,X maleV B Chernykh, S V Vyatkina, V G Antonenko, et al.
Genetika|January 27, 2018
[Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders]O L Mironovich, E A Bliznetz, T G Markova, et al.
Journal of Biomedical Materials Research. Part A|November 28, 2012
In vitro and in vivo studies on nanocrystalline Ti fabricated by equal channel angular pressing with microcrystalline CP Ti as controlF L Nie, Y F Zheng, S C Wei, et al.
Vestnik Otorinolaringologii|August 17, 2018
[Epidemiology of hearing loss in children of the first year of life]S S Chibisova, T G Markova, N N Alekseeva, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21S M Ismailov, V P Fedotov, E L Dadali, et al.
Vestnik Oftalmologii|October 26, 2022
[Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation)]I V Zolnikova, S V Milash, R A Zinchenko, et al.
Pageof 6