Search Results - "Porhanova, Nathalia V"

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  1. 1
    High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients

    High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients by Suspitsin, Evgeny N, Sherina, Nathalia Yu, Ponomariova, Daria N, Sokolenko, Anna P, Iyevleva, Aglaya G, Gorodnova, Tatyana V, Zaitseva, Olga A, Yatsuk, Olga S, Togo, Alexandr V, Tkachenko, Nathalia N, Shiyanov, Grigory A, Lobeiko, Oksana S, Krylova, Nadezhda Yu, Matsko, Dmitry E, Maximov, Sergey Ya, Urmancheyeva, Adel F, Porhanova, Nathalia V, Imyanitov, Evgeny N

    Published in Hereditary cancer in clinical practice (25-02-2009)
    “…A significant portion of ovarian cancer (OC) cases is caused by germ-line mutations in BRCA1 or BRCA2 genes. BRCA testing is cheap in populations with founder…”
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  2. 2
    Ovarian cancer patient with germline mutations in both BRCA1 and NBN genes

    Ovarian cancer patient with germline mutations in both BRCA1 and NBN genes by Porhanova, Nathalia V, Sokolenko, Anna P, Sherina, Nathalia Yu, Ponomariova, Daria N, Tkachenko, Nathalia N, Matsko, Dmitry E, Imyanitov, Evgeny N

    Published in Cancer genetics and cytogenetics (15-10-2008)
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  3. 3
    Ovarian cancer patient with germline mutations in both BRCA1 and NBN genes

    Ovarian cancer patient with germline mutations in both BRCA1 and NBN genes by Porhanova, Nathalia V, Sokolenko, Anna P, Sherina, Nathalia Yu, Ponomariova, Daria N, Tkachenko, Nathalia N, Matsko, Dmitry E, Imyanitov, Evgeny N

    Published in Cancer genetics and cytogenetics (15-10-2008)
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