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Page 1
Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss.
J Pers Med. 2022 Nov 4;12(11):1843. doi: 10.3390/jpm12111843.
J Pers Med. 2022.
PMID: 36579563
Free PMC article.
Ehlers-Danlos syndrome kyphoscoliotic type 2 caused by mutations in the FKBP14 gene: an analysis of five cases.
Semyachkina AN, Nikolaeva EA, Galeeva NM, Polyakov AV, Kurnikova MA, Belova VА, Shulyakova IV, Dantsev IS, Dzhivanshiryan GV.
Semyachkina AN, et al. Among authors: galeeva nm.
F1000Res. 2021 Jun 25;10:502. doi: 10.12688/f1000research.52268.1. eCollection 2021.
F1000Res. 2021.
PMID: 34504686
Free PMC article.
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Spectrum of Genes for Non-GJB2-Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel.
Shatokhina O, Galeeva N, Stepanova A, Markova T, Lalayants M, Alekseeva N, Tavarkiladze G, Markova T, Bessonova L, Petukhova M, Guseva D, Anisimova I, Polyakov A, Ryzhkova O, Bliznetz E.
Shatokhina O, et al. Among authors: galeeva n.
Int J Mol Sci. 2022 Dec 12;23(24):15748. doi: 10.3390/ijms232415748.
Int J Mol Sci. 2022.
PMID: 36555390
Free PMC article.
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Clinical and genetic characterization of three Russian patients with pycnodysostosis due to pathogenic variants in the CTSK gene.
Markova TV, Kenis V, Melchenko E, Guseva D, Osipova D, Galeeva N, Nagornova T, Dadali EL.
Markova TV, et al. Among authors: galeeva n.
Mol Genet Genomic Med. 2022 May;10(5):e1904. doi: 10.1002/mgg3.1904. Epub 2022 Mar 21.
Mol Genet Genomic Med. 2022.
PMID: 35315254
Free PMC article.
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