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[The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances]

Autor: Lalaiants, M. R., Markova, T. G., Bakhshinian, V. V., Bliznets, E. A., Poliakov, A. V., Tavartikiladze, G. A.

Publikováno v: Scopus-Elsevier

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::546dff55a1fca6fb73368136c8a34fa5
http://www.scopus.com/inward/record.url?eid=2-s2.0-84906309743&partnerID=MN8TOARS

[Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness]

Autor: Bliznets, E. A., Galkina, V. A., Matiushchenko, G. N., Kisina, A. G., Markova, T. G., Poliakov, A. V.

Publikováno v: Scopus-Elsevier

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::76031a80d9eee86e0cf71beb83ae907b
http://www.scopus.com/inward/record.url?eid=2-s2.0-84862280645&partnerID=MN8TOARS

[Hearing loss due to mutations or lack of the gene coding protein stereocillin].

Autor: Markova TG; National Resarch Center for Audiology and Hearing Rehabilitation, Moscow, Russia.; Russian Medical Academy of Postdoctoral Education of the Ministry of Health of Russia, Moscow, Russia., Alekseeva NN; National Resarch Center for Audiology and Hearing Rehabilitation, Moscow, Russia.; Russian Medical Academy of Postdoctoral Education of the Ministry of Health of Russia, Moscow, Russia., Mironovich OL; Academician N.P. Bochkov Medical and Genetic Research Center, Moscow, Russia., Bliznets EA; Academician N.P. Bochkov Medical and Genetic Research Center, Moscow, Russia., Lalayants MR; National Resarch Center for Audiology and Hearing Rehabilitation, Moscow, Russia.; Russian Medical Academy of Postdoctoral Education of the Ministry of Health of Russia, Moscow, Russia., Polyakov AV; Academician N.P. Bochkov Medical and Genetic Research Center, Moscow, Russia., Tavartkiladze GA; National Resarch Center for Audiology and Hearing Rehabilitation, Moscow, Russia.; Russian Medical Academy of Postdoctoral Education of the Ministry of Health of Russia, Moscow, Russia.

Publikováno v: Vestnik otorinolaringologii [Vestn Otorinolaringol] 2020; Vol. 85 (2), pp. 14-20.

[New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance].

Autor: Bliznets EA, Makienko ON, Okuneva EG, Markova TG, Poliakov AV

Publikováno v: Genetika [Genetika] 2014 Apr; Vol. 50 (4), pp. 474-80.