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Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. Online.
Claes K, Machackova E, De Vos M, Mortier G, De Paepe A, Messiaen L. Claes K, et al. Among authors: machackova e. Hum Mutat. 1999;13(3):256. doi: 10.1002/(SICI)1098-1004(1999)13:3<256::AID-HUMU12>3.0.CO;2-M. Hum Mutat. 1999. PMID: 10090482
[The clinical importance of a genetic analysis of moderate-risk cancer susceptibility genes in breast and other cancer patients from the Czech Republic].
Pohlreich P, Kleibl Z, Kleiblová P, Janatová M, Soukupová J, Macháčková E, Házová J, Vašíčková P, Sťahlová Hrabincová E, Navrátilová M, Svoboda M, Foretová L. Pohlreich P, et al. Among authors: machackova e. Klin Onkol. 2012;25 Suppl:S59-66. Klin Onkol. 2012. PMID: 22920209 Review. Czech.
[Breast cancer in monozygotic twins].
Hladíková A, Plevová P, Macháčková E. Hladíková A, et al. Among authors: machackova e. Klin Onkol. 2013;26(3):213-7. doi: 10.14735/amko2013213. Klin Onkol. 2013. PMID: 23763326 Czech.
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