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Page 1
Clinical and Genetic Characteristics of COL2A1-Associated Skeletal Dysplasias in 60 Russian Patients: Part I.
Genes (Basel). 2022 Jan 13;13(1):137. doi: 10.3390/genes13010137.
Genes (Basel). 2022.
PMID: 35052477
Free PMC article.
Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population.
Glotov OS, Savostyanov KV, Nagornova TS, Chernov AN, Fedyakov MA, Raspopova AN, Krasnoukhov KN, Danilov LG, Moiseeva NV, Kalinin RS, Tsai VV, Eismont YA, Voinova VY, Vitebskaya AV, Gurkina EY, Kuzenkova LM, Sosnina IB, Pushkov AA, Zhanin IS, Zakharova EY.
Glotov OS, et al. Among authors: nagornova ts.
Int J Mol Sci. 2022 Oct 26;23(21):12976. doi: 10.3390/ijms232112976.
Int J Mol Sci. 2022.
PMID: 36361766
Free PMC article.
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Does the c.-14C>T Mutation in the IFITM5 Gene Provide Identical Phenotypes for Osteogenesis Imperfecta Type V? Data from Russia and a Literature Review.
Tyurin A, Merkuryeva E, Zaripova A, Markova T, Nagornova T, Dantsev I, Nadyrshina D, Zakharova E, Khusainova R.
Tyurin A, et al. Among authors: nagornova t.
Biomedicines. 2022 Sep 22;10(10):2363. doi: 10.3390/biomedicines10102363.
Biomedicines. 2022.
PMID: 36289625
Free PMC article.
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Rare IFT140-Associated Phenotype of Cranioectodermal Dysplasia and Features of Diagnostic Journey in Patients with Suspected Ciliopathies.
Sharova M, Markova T, Sumina M, Petukhova M, Bulakh M, Ryzhkova O, Nagornova T, Ionova S, Marakhonov A, Dadali E, Kutsev S.
Sharova M, et al. Among authors: nagornova t.
Genes (Basel). 2023 Jul 28;14(8):1553. doi: 10.3390/genes14081553.
Genes (Basel). 2023.
PMID: 37628605
Free PMC article.
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