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Vestnik Otorinolaringologii|May 1, 2014
[The universal audiological screening of newborn infants: achievements and challenges]S S Chibisova, E R Tsygankova, T G Markova, et al.Vestnik Otorinolaringologii|December 13, 2006
[Genetic screening among children with congenital and early childhood hearing loss]T G Markova, M V Nekrasovan V, I A Shagina, et al.Vestnik Otorinolaringologii|July 2, 2011
[The results of audiological examination of children presenting with sensorineural loss of hearing due to GJB2 gene mutations during the first year of life]M R Lalaiants, E A Bliznets, T G Markova, et al.Vestnik Otorinolaringologii|May 24, 2016
[The Russian and international experience with the implementation of the programs of universal audiological screening of the newborn infants]G A Tavartkiladze, T G Markova, S S Chibisova, et al.Vestnik Otorinolaringologii|March 11, 2022
[Hearing loss due to mutations in the genes responsible for Usher syndrome]T G Markova, N N Alekseeva, O A Belov, et al.Genetika|February 27, 2015
[New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance]E A Bliznets, O N Makienko, E G Okuneva, et al.Vestnik Otorinolaringologii|June 19, 2010
[Genetic screening for hearing disorders in newborn infants in combination with audiological screening]G A Tavartkiladze, A V Poliakov, T G Markova, et al.Vestnik Otorinolaringologii|May 1, 2014
[Johanson-Blizzard syndrome: audiological features and results of cochlear implantation]T I Chugunova, V V Bakhshinian, T G Markova, et al.Vestnik Otorinolaringologii|December 28, 2002
[DNA diagnosis in congenital and early childhood hypoacusis and deafness]T G Markova, S M Megrelishvilli, N G Zaĭtseva, et al.Vestnik Otorinolaringologii|September 7, 2012
[Diagnostics of keratitis-ichthyosis-deafness syndrome (KID- syndrome)]T G Markova, N B Brazhkina, E V Bliznets, et al.Pageof 4