Search Results - Balinova, Natalia V. 

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  1. 1
    High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients

    High frequency of complex CFTR alleles associated with c.1521_1523delCTT (F508del) in Russian cystic fibrosis patients by Petrova, Nika V, Kashirskaya, Nataliya Y, Vasilyeva, Tatyana A, Balinova, Natalia V, Marakhonov, Andrey V, Kondratyeva, Elena I, Zhekaite, Elena K, Voronkova, Anna Y, Kutsev, Sergey I, Zinchenko, Rena A

    Published in BMC genomics
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    Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population

    Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population by Petrova, Nika V, Marakhonov, Andrey V, Balinova, Natalia V, Abrukova, Anna V, Konovalov, Fedor A, Kutsev, Sergey I, Zinchenko, Rena A

    Published in Genes
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    COMMON ANCESTORS OF TURKIC-SPEAKING PEOPLES: GENETIC ASPECTS

    COMMON ANCESTORS OF TURKIC-SPEAKING PEOPLES: GENETIC ASPECTS by Spitsyna, Nailya Kh, Balinova, Natalia V. 

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