Search Results - Khmelkova, Darya N

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  1. 1
    An MSH6 germline pathogenic variant p.Gly162Ter associated with Lynch syndrome

    An MSH6 germline pathogenic variant p.Gly162Ter associated with Lynch syndrome by Vostrukhina, Olga A., Mirlina, Elena D., Khmelkova, Darya N., Butrovich, Galina M., Shakhmatova, Alexandra D., Kil, Yury V., Polyatskin, Yliya L., Artemyeva, Anna S., Gulyaev, Alexey V., Verbenko, Valery N.

    Published in Human genome variation
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    Expanding the Russian allele frequency reference via cross-laboratory data integration: insights from 7452 exome samples

    Expanding the Russian allele frequency reference via cross-laboratory data integration: insights from 7452 exome samples by Barbitoff, Yury A, Khmelkova, Darya N, Pomerantseva, Ekaterina A, Slepchenkov, Aleksandr V, Zubashenko, Nikita A, Mironova, Irina V, Kaimonov, Vladimir S, Polev, Dmitrii E, Tsay, Victoria V, Glotov, Andrey S, Aseev, Mikhail V, Shcherbak, Sergey G, Glotov, Oleg S, Isaev, Arthur A, Predeus, Alexander V

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