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	1.	Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia). [electronic resource] by Сhurbanov, Alexander Y Karafet, Tatiana M Morozov, Igor V Mikhalskaia, Valeriia Yu Zytsar, Marina V Bondar, Alexander A Posukh, Olga L Producer: 20160906 In: PloS one vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Unique Mutational Spectrum of the [electronic resource] by Posukh, Olga L Zytsar, Marina V Bady-Khoo, Marita S Danilchenko, Valeria Yu Maslova, Ekaterina A Barashkov, Nikolay A Bondar, Alexander A Morozov, Igor V Maximov, Vladimir N Voevoda, Michael I Producer: 20191226 In: Genes vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia. [electronic resource] by Zytsar, Marina V Barashkov, Nikolay A Bady-Khoo, Marita S Shubina-Olejnik, Olga A Danilenko, Nina G Bondar, Alexander A Morozov, Igor V Solovyev, Aisen V Danilchenko, Valeriia Yu Maximov, Vladimir N Posukh, Olga L Producer: 20190415 In: BMC medical genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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