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Suspitsin EN, Sherina NY, Ponomariova DN, et al. High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients. Hered Cancer Clin Pract. 2009;7(1):5doi: 10.1186/1897-4287-7-5.
Suspitsin, E. N., Sherina, N. Y., Ponomariova, D. N., Sokolenko, A. P., Iyevleva, A. G., Gorodnova, T. V., Zaitseva, O. A., Yatsuk, O. S., Togo, A. V., Tkachenko, N. N., Shiyanov, G. A., Lobeiko, O. S., Krylova, N. Y., Matsko, D. E., Maximov, S. Y., Urmancheyeva, A. F., Porhanova, N. V., & Imyanitov, E. N. (2009). High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients. Hereditary cancer in clinical practice, 7(1), 5. https://doi.org/10.1186/1897-4287-7-5
Suspitsin, Evgeny N, et al. "High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients." Hereditary cancer in clinical practice vol. 7,1 (2009): 5. doi: https://doi.org/10.1186/1897-4287-7-5
Suspitsin EN, Sherina NY, Ponomariova DN, Sokolenko AP, Iyevleva AG, Gorodnova TV, Zaitseva OA, Yatsuk OS, Togo AV, Tkachenko NN, Shiyanov GA, Lobeiko OS, Krylova NY, Matsko DE, Maximov SY, Urmancheyeva AF, Porhanova NV, Imyanitov EN. High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients. Hered Cancer Clin Pract. 2009 Feb 25;7(1):5. doi: 10.1186/1897-4287-7-5. PMID: 19338682; PMCID: PMC2664323.
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