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Real-World Data on Detection of Germline and Somatic Pathogenic/Likely Pathogenic Variants in BRCA1/2 and Other Susceptibility Genes in Ovarian Cancer Patients Using Next Generation Sequencing.
Stegel V, Blatnik A, Škof E, Dragoš VŠ, Krajc M, Gregorič B, Škerl P, Strojnik K, Klančar G, Banjac M, Žgajnar J, Ravnik M, Novaković S. Stegel V, et al. Among authors: blatnik a. Cancers (Basel). 2022 Mar 10;14(6):1434. doi: 10.3390/cancers14061434. Cancers (Basel). 2022. PMID: 35326583 Free PMC article.
Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin.
Krivokuca A, Dragos VS, Stamatovic L, Blatnik A, Boljevic I, Stegel V, Rakobradovic J, Skerl P, Jovandic S, Krajc M, Magic MB, Novakovic S. Krivokuca A, et al. Among authors: blatnik a. Fam Cancer. 2018 Apr;17(2):179-185. doi: 10.1007/s10689-017-0022-x. Fam Cancer. 2018. PMID: 28685474
BAP1-defficient breast cancer in a patient with BAP1 cancer syndrome.
Blatnik A, Ribnikar D, Šetrajčič Dragoš V, Novaković S, Stegel V, Grčar Kuzmanov B, Boc N, Perić B, Škerl P, Klančar G, Krajc M. Blatnik A, et al. Breast Cancer. 2022 Sep;29(5):921-927. doi: 10.1007/s12282-022-01354-0. Epub 2022 Apr 5. Breast Cancer. 2022. PMID: 35381901 Free PMC article.
56 results