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Page 1
The spectrum and incidence of BRCA1 pathogenic mutations in Slovak breast/ovarian cancer families.
Neoplasma. 2007;54(2):137-42.
Neoplasma. 2007.
PMID: 17319787
Comprehensive genetic characterization of hereditary breast/ovarian cancer families from Slovakia.
Konecny M, Milly M, Zavodna K, Weismanova E, Gregorova J, Mlkva I, Ilencikova D, Kausitz J, Bartosova Z.
Konecny M, et al. Among authors: mlkva i.
Breast Cancer Res Treat. 2011 Feb;126(1):119-30. doi: 10.1007/s10549-010-1325-x. Epub 2011 Jan 4.
Breast Cancer Res Treat. 2011.
PMID: 21203900
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Identification of rare complete BRCA1 gene deletion using a combination of SNP haplotype analysis, MLPA and array-CGH techniques.
Konecny M, Zavodna K, Vranova V, Vizvaryova M, Weismanova E, Mlkva I, Kuglik P, Kausitz J, Bartosova Z.
Konecny M, et al. Among authors: mlkva i.
Breast Cancer Res Treat. 2008 Jun;109(3):581-3. doi: 10.1007/s10549-007-9670-0. Epub 2007 Jul 28.
Breast Cancer Res Treat. 2008.
PMID: 17661172
No abstract available.
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STK11/LKB1 germline mutations in the first Peutz-Jeghers syndrome patients identified in Slovakia.
Bartosova Z, Zavodna K, Krivulcik T, Usak J, Mlkva I, Kruzliak T, Hromec J, Usakova V, Kopecka I, Veres P, Bartosova Z, Bujalkova M.
Bartosova Z, et al. Among authors: mlkva i.
Neoplasma. 2007;54(2):101-7.
Neoplasma. 2007.
PMID: 17319781
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[Possibilities of genetic diagnostics of intestine tumour and inflammatory diseases in Slovakia].
Desatová B, Bátovský M, Mľkva I.
Desatová B, et al. Among authors: mlkva i.
Vnitr Lek. 2013 Nov;59(11):977-80.
Vnitr Lek. 2013.
PMID: 24279441
Review.
Czech.
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[Genetics of Colorectal Tumorigenesis (Possibilities of Testing and Screening Prediction of Hereditary Form of Colorectal Cancer--Lynch Syndrome)].
Mľkva I.
Mľkva I.
Klin Onkol. 2016;29 Suppl 1:S55-61.
Klin Onkol. 2016.
PMID: 26691943
Czech.
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