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[Genetic screening for hearing disorders in newborn infants in combination with audiological screening].
Vestn Otorinolaringol. 2010;(3):15-8.
Vestn Otorinolaringol. 2010.
PMID: 20559245
Russian.
[The results of audiological examination of children presenting with sensorineural loss of hearing due to GJB2 gene mutations during the first year of life].
Lalaiants MR, Bliznets EA, Markova TG, Poliakov AV, Tavartkiladze GA.
Lalaiants MR, et al. Among authors: bliznets ea.
Vestn Otorinolaringol. 2011;(3):31-5.
Vestn Otorinolaringol. 2011.
PMID: 21720291
Russian.
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[The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances].
Lalaiants MR, Markova TG, Bakhshinian VV, Bliznets EA, Poliakov AV, Tavartikiladze GA.
Lalaiants MR, et al. Among authors: bliznets ea.
Vestn Otorinolaringol. 2014;(2):37-43.
Vestn Otorinolaringol. 2014.
PMID: 24781170
Russian.
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[Hearing loss due to mutations or lack of the gene coding protein stereocillin].
Markova TG, Alekseeva NN, Mironovich OL, Bliznets EA, Lalayants MR, Polyakov AV, Tavartkiladze GA.
Markova TG, et al. Among authors: bliznets ea.
Vestn Otorinolaringol. 2020;85(2):14-20. doi: 10.17116/otorino20208502114.
Vestn Otorinolaringol. 2020.
PMID: 32476383
Russian.
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[Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness].
Bliznets EA, Galkina VA, Matiushchenko GN, Kisina AG, Markova TG, Poliakov AV.
Bliznets EA, et al.
Genetika. 2012 Jan;48(1):112-24.
Genetika. 2012.
PMID: 22567861
Russian.
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[The mutation spectrum of the GJB2 gene in Belarussian patients with hearing loss. Results of pilot genetic screening of hearing impairment in newborns].
Bliznets EA, Marcul' DN, Khorov OG, Markova TG, Poliakov AV.
Bliznets EA, et al.
Genetika. 2014 Feb;50(2):214-21.
Genetika. 2014.
PMID: 25711030
Russian.
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[New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance].
Bliznets EA, Makienko ON, Okuneva EG, Markova TG, Poliakov AV.
Bliznets EA, et al.
Genetika. 2014 Apr;50(4):474-80.
Genetika. 2014.
PMID: 25715449
Russian.
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[OTOF-related auditory neuropathy spectrum disorder].
Lalayants MR, Mironovich OL, Bliznets EA, Markova TG, Polyakov AV, Tavartkiladze GA.
Lalayants MR, et al. Among authors: bliznets ea.
Vestn Otorinolaringol. 2020;85(2):21-25. doi: 10.17116/otorino20208502121.
Vestn Otorinolaringol. 2020.
PMID: 32476384
Russian.
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