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Search Results - Bliznetz, E. A
Search Results - Bliznetz, E. A
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Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population
by
Markova, T.G.
,
Alekseeva, N.N.
,
Mironovich, O.L.
,
Galeeva, N.M.
,
Lalayants, M.R.
,
Bliznetz, E.A.
,
Chibisova, S.S.
,
Polyakov, A.V.
,
Tavartkiladze, G.A.
Published in
International journal of pediatric otorhinolaryngology
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Early audiological phenotype in patients with mutations in the USH2A gene
by
Markova, T.G.
,
Lalayants, M.R.
,
Alekseeva, N.N.
,
Ryzhkova, O.P.
,
Shatokhina, O.L.
,
Galeeva, N.M.
,
Bliznetz, E.A.
,
Weener, M.E.
,
Belov, O.A.
,
Chibisova, S.S.
,
Polyakov, A.V.
,
Tavartkiladze, G.A.
Published in
International journal of pediatric otorhinolaryngology
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New recurrent large deletion, encompassing both GJB2 and GB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive mode of inheritance
by
Bliznetz, E. A
,
Makienko, O. N
,
Okuneva, E. G
,
Markova, T. G
,
Polyakov, A. V
Published in
Russian journal of genetics
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Spectrum of the GJB2 mutations in Belarussian patients with hearing loss. Findings of pilot genetic screening of hearing impairment in newborns
by
Bliznetz, E. A
,
Martsul, D. N
,
Khorov, O. G
,
Markova, T. G
,
Polyakov, A. V
Published in
Russian journal of genetics
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DNA copy number analysis of the DFNB1 hereditary hearing loss locus
by
Bliznetz, E. A.
,
Kanivets, I. V.
,
Polyakov, A. V.
Published in
Russian journal of genetics
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Molecular Genetic Causes and Clinical Description of Branchio-Oto-renal Syndrome
by
Mironovich, O. L.
,
Bliznetz, E. A.
,
Markova, T. G.
,
Alekseeva, N. N.
,
Golybeva, T. I.
,
Ryzhkova, O. P.
,
Polyakov, A. V.
Published in
Russian journal of genetics
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Polymorphism of CAG Repeats in Exon 1 of the Androgen Receptor Gene in Russian Men with Various Forms of Pathozoospermia
by
Melikyan, L. P.
,
Bliznetz, E. A.
,
Polyakov, A. V.
,
Mironovich, O. L.
,
Kuznetsova, I. A.
,
Sorokina, T. M.
,
Shtaut, M. I.
,
Sedova, A. O.
,
Kurilo, L. F.
,
Solovova, O. A.
,
Chernykh, V. B.
Published in
Russian journal of genetics
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Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders
by
Mironovich, O. L.
,
Bliznetz, E. A.
,
Markova, T. G.
,
Geptner, E. N.
,
Lalayants, M. R.
,
Zelikovich, E. I.
,
Tavartkiladze, G. A.
,
Polyakov, A. V.
Published in
Russian journal of genetics
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Changes in the connexin 26 gene (GJB2) in Russian patients with hearing loss: Results of long-term molecular diagnostics of hereditary nonsyndromic hearing loss
by
Bliznetz, E. A.
,
Galkina, V. A.
,
Matyushchenko, G. N.
,
Kisina, A. G.
,
Markova, T. G.
,
Polyakov, A. V.
Published in
Russian journal of genetics
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Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649)
by
Knappskog, Stian
,
Gansmo, Liv B
,
Dibirova, Khadizha
,
Metspalu, Andres
,
Cybulski, Cezary
,
Peterlongo, Paolo
,
Aaltonen, Lauri
,
Vatten, Lars
,
Romundstad, Pål
,
Hveem, Kristian
,
Devilee, Peter
,
Evans, Gareth D
,
Lin, Dongxin
,
Van Camp, Guy
,
Manolopoulos, Vangelis G
,
Osorio, Ana
,
Milani, Lili
,
Ozcelik, Tayfun
,
Zalloua, Pierre
,
Mouzaya, Francis
,
Bliznetz, Elena
,
Balanovska, Elena
,
Pocheshkova, Elvira
,
Kučinskas, Vaidutis
,
Atramentova, Lubov
,
Nymadawa, Pagbajabyn
,
Titov, Konstantin
,
Lavryashina, Maria
,
Yusupov, Yuldash
,
Bogdanova, Natalia
,
Koshel, Sergey
,
Zamora, Jorge
,
Wedge, David C
,
Charlesworth, Deborah
,
Dörk, Thilo
,
Balanovsky, Oleg
,
Lønning, Per E
Published in
Oncotarget
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