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Gurinova Ee

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A novel homozygous mutation causing hereditary tyrosinemia type I in yakut patient in russia: case report.

2016 Wiadomości lekarskie (Warsaw Poland)
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Cochlear implantation in a child with congenital sensorineural deafness due to 35 DELG mutation in GJB2 (connexin 26) gene

2009 Vestnik otorinolaringologii
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[The clinical-genealogic and molecular-genetic characteristics of oculopharyngeal muscular dystrophy in the Republic of Sakha (Yakutia)].

2008 Zhurnal Nevrologii I Psikhiatrii Imeni S S Korsakova
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