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A V Polyakov

Showing results (51-60 of 56) with videos related to

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Vestnik Oftalmologii|October 6, 2017
[Molecular genetic diagnosis of Stargardt disease]N L Sheremet, N V Zhorzholadze, I A Ronzina, et al.
International Journal of Pediatric Otorhinolaryngology|April 22, 2022
Early audiological phenotype in patients with mutations in the USH2A geneT G Markova, M R Lalayants, N N Alekseeva, et al.
Frontiers in Genetics|May 16, 2022
Genetic Landscape of Nephropathic Cystinosis in Russian ChildrenK V Savostyanov, A A Pushkov, O A Shchagina, et al.
Problemy Endokrinologii|February 5, 2026
Does everyone need to take vitamin D? High prevalence of CYP24A1 deficiency in the Russian populationK S Kulikova, S V Papizh, A V Polyakov, et al.
BMC Medical Genetics|March 23, 2019
Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North CaucasusN V Petrova, N Y Kashirskaya, D K Saydaeva, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Comparative cytogenetics of hamsters of the genus CalomyscusA S Graphodatsky, O V Sablina, M N Meyer, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Vestnik Oftalmologii|October 6, 2017
[Molecular genetic diagnosis of Stargardt disease]N L Sheremet, N V Zhorzholadze, I A Ronzina, et al.
International Journal of Pediatric Otorhinolaryngology|April 22, 2022
Early audiological phenotype in patients with mutations in the USH2A geneT G Markova, M R Lalayants, N N Alekseeva, et al.
Frontiers in Genetics|May 16, 2022
Genetic Landscape of Nephropathic Cystinosis in Russian ChildrenK V Savostyanov, A A Pushkov, O A Shchagina, et al.
Problemy Endokrinologii|February 5, 2026
Does everyone need to take vitamin D? High prevalence of CYP24A1 deficiency in the Russian populationK S Kulikova, S V Papizh, A V Polyakov, et al.
BMC Medical Genetics|March 23, 2019
Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North CaucasusN V Petrova, N Y Kashirskaya, D K Saydaeva, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Comparative cytogenetics of hamsters of the genus CalomyscusA S Graphodatsky, O V Sablina, M N Meyer, et al.
Pageof 6