T G Markova - JoVE Visualize

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Genetika|February 26, 2015

[The mutation spectrum of the GJB2 gene in Belarussian patients with hearing loss. Results of pilot genetic screening of hearing impairment in newborns]E A Bliznets, D N Marcul', O G Khorov, et al.

Vestnik Otorinolaringologii|May 1, 2014

[The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances]M R Lalaiants, T G Markova, V V Bakhshinian, et al.

Genetika|May 10, 2012

[Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness]E A Bliznets, V A Galkina, G N Matiushchenko, et al.

International Journal of Pediatric Otorhinolaryngology|January 27, 2016

Phenotype in a patient with p.D50N mutation in GJB2 gene resemble both KID and Clouston syndromesT G Markova, N B Brazhkina, E A Bliznech, et al.

Vestnik Otorinolaringologii|June 2, 2020

[OTOF-related auditory neuropathy spectrum disorder]M R Lalayants, O L Mironovich, E A Bliznets, et al.

Vestnik Otorinolaringologii|January 17, 2017

[Application of the mathematical model for prognosis in the rehabilitation of children after cochlear implantation]I P Petrova, E A Balashova, M V Goykhburg, et al.

Vestnik Otorinolaringologii|June 2, 2020

[Hearing loss due to mutations or lack of the gene coding protein stereocillin]T G Markova, N N Alekseeva, O L Mironovich, et al.

Genetika|January 27, 2018

[Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders]O L Mironovich, E A Bliznetz, T G Markova, et al.

Vestnik Otorinolaringologii|August 17, 2018

[Epidemiology of hearing loss in children of the first year of life]S S Chibisova, T G Markova, N N Alekseeva, et al.

International Journal of Pediatric Otorhinolaryngology|July 25, 2020

Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian populationT G Markova, N N Alekseeva, O L Mironovich, et al.

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Showing results (21-30 of 35) with videos related to

Sort By:

Pageof 4

Genetika|February 26, 2015

[The mutation spectrum of the GJB2 gene in Belarussian patients with hearing loss. Results of pilot genetic screening of hearing impairment in newborns]E A Bliznets, D N Marcul', O G Khorov, et al.

Vestnik Otorinolaringologii|May 1, 2014

[The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances]M R Lalaiants, T G Markova, V V Bakhshinian, et al.

Genetika|May 10, 2012

[Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness]E A Bliznets, V A Galkina, G N Matiushchenko, et al.

International Journal of Pediatric Otorhinolaryngology|January 27, 2016

Phenotype in a patient with p.D50N mutation in GJB2 gene resemble both KID and Clouston syndromesT G Markova, N B Brazhkina, E A Bliznech, et al.

Vestnik Otorinolaringologii|June 2, 2020

[OTOF-related auditory neuropathy spectrum disorder]M R Lalayants, O L Mironovich, E A Bliznets, et al.

Vestnik Otorinolaringologii|January 17, 2017

[Application of the mathematical model for prognosis in the rehabilitation of children after cochlear implantation]I P Petrova, E A Balashova, M V Goykhburg, et al.

Vestnik Otorinolaringologii|June 2, 2020

[Hearing loss due to mutations or lack of the gene coding protein stereocillin]T G Markova, N N Alekseeva, O L Mironovich, et al.

Genetika|January 27, 2018

[Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders]O L Mironovich, E A Bliznetz, T G Markova, et al.

Vestnik Otorinolaringologii|August 17, 2018

[Epidemiology of hearing loss in children of the first year of life]S S Chibisova, T G Markova, N N Alekseeva, et al.

International Journal of Pediatric Otorhinolaryngology|July 25, 2020

Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian populationT G Markova, N N Alekseeva, O L Mironovich, et al.

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