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European Journal of Human Genetics
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Letter
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  • Letter
  • Published: 25 March 2001

Letter

Letter

  • Anna Anichkina1,
  • Tatiana Kulenich1,
  • Sergey Zinchenko1,
  • Irena Shagina1,
  • Aleksander Polyakov1,
  • Evgenii Ginter1,
  • Oleg Evgrafov1,
  • Tatiana Viktorova2 &
  • …
  • Elza Khusnitdonova2 

European Journal of Human Genetics volume 9, page 151 (2001)Cite this article

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  • 12 Citations

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References

  1. Gasparini P et al:. High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delG. Eur J Hum Genet 2000 8: 19–23.

    Article  CAS  Google Scholar 

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Authors and Affiliations

  1. Research Center for Medical Genetics, Moscow, Russia

    Anna Anichkina, Tatiana Kulenich, Sergey Zinchenko, Irena Shagina, Aleksander Polyakov, Evgenii Ginter & Oleg Evgrafov

  2. Ufa Research Center, Ufa, Russia

    Tatiana Viktorova & Elza Khusnitdonova

Authors
  1. Anna Anichkina
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  2. Tatiana Kulenich
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  3. Sergey Zinchenko
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  4. Irena Shagina
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  5. Aleksander Polyakov
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  6. Evgenii Ginter
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  7. Oleg Evgrafov
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  8. Tatiana Viktorova
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  9. Elza Khusnitdonova
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Cite this article

Anichkina, A., Kulenich, T., Zinchenko, S. et al. Letter. Eur J Hum Genet 9, 151 (2001). https://doi.org/10.1038/sj.ejhg.5200596

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  • Published: 25 March 2001

  • Issue date: 01 February 2001

  • DOI: https://doi.org/10.1038/sj.ejhg.5200596

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This article is cited by

  • Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia

    • Lilya U Dzhemileva
    • Nikolay A Barashkov
    • Elza K Khusnutdinova

    Journal of Human Genetics (2010)

  • First molecular screening of deafness in the Altai Republic population

    • Olga Posukh
    • Nathalie Pallares-Ruiz
    • Anne-Françoise Roux

    BMC Medical Genetics (2005)

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European Journal of Human Genetics (Eur J Hum Genet)

ISSN 1476-5438 (online)

ISSN 1018-4813 (print)

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