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List of works by Elena Bliznetz

Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss

scientific article published in 2022

Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect.

scientific article

Hidden X chromosomal mosaicism in a 46,XX male

scientific article published on 11 September 2009

Molecular-genetic causes for the high frequency of phenylketonuria in the population from the North Caucasus.

scientific article published in August 2018

Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions

scientific article published on 13 April 2017

[Diagnostics of keratitis-ichthyosis-deafness syndrome (KID- syndrome)]

article published in 2012

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

scientific article published on 01 January 2020

[OTOF-related auditory neuropathy spectrum disorder]

scientific article published on 01 January 2020

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