Found: 5
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Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss.
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- Journal of Personalized Medicine, 2022, v. 12, n. 11, p. 1843, doi. 10.3390/jpm12111843
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- Article
Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 24, p. 15748, doi. 10.3390/ijms232415748
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- Article
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia.
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- Human Genetics, 2022, v. 141, n. 3/4, p. 697, doi. 10.1007/s00439-021-02405-w
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- Article
Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect.
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- European Journal of Human Genetics, 2009, v. 17, n. 5, p. 664, doi. 10.1038/ejhg.2008.234
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- Article
Molecular-genetic causes for the high frequency of phenylketonuria in the population from the North Caucasus.
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- PLoS ONE, 2018, v. 13, n. 8, p. 1, doi. 10.1371/journal.pone.0201489
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- Article