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2020 | 1 |
2022 | 3 |
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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.
Glycated hemoglobin level dynamics in COVID-19 survivors: 12 months follow-up study after discharge from hospital.
Shestakova M, Kononenko I, Kalmykovа Z, Markova T, Kaplun E, Lysenko M, Mokrysheva N.
Shestakova M, et al. Among authors: markova t.
PLoS One. 2022 Nov 9;17(11):e0275381. doi: 10.1371/journal.pone.0275381. eCollection 2022.
PLoS One. 2022.
PMID: 36350895
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: markova 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: markova 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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Identification of a Novel de Novo Variant in the SYT2 Gene Causing a Rare Type of Distal Hereditary Motor Neuropathy.
Mironovich O, Dadali E, Malmberg S, Markova T, Ryzhkova O, Poliakov A.
Mironovich O, et al. Among authors: markova t.
Genes (Basel). 2020 Oct 22;11(11):1238. doi: 10.3390/genes11111238.
Genes (Basel). 2020.
PMID: 33105646
Free PMC article.
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