Your search returned 7 results.

Results
	1.	Haplotype analysis of two recurrent genomic rearrangements in the BRCA1 gene suggests they are founder mutations for the Greek population. [electronic resource] by Pertesi, M Konstantopoulou, I Yannoukakos, D Producer: 20130822 In: Clinical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Hereditary cancer predisposition syndromes and preimplantation genetic diagnosis: where are we now? [electronic resource] by Konstantopoulou, I Pertesi, M Fostira, F Grivas, A Yannoukakos, D Producer: 20100427 In: Journal of B.U.ON. : official journal of the Balkan Union of Oncology vol. 14 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	3.	Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases. [electronic resource] by Armaou, S Pertesi, M Fostira, F Thodi, G Athanasopoulos, P S Kamakari, S Athanasiou, A Gogas, H Yannoukakos, D Fountzilas, G Konstantopoulou, I Producer: 20090708 In: British journal of cancer vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation. [electronic resource] by Apostolou, P Pertesi, M Aleporou-Marinou, V Dimitrakakis, C Papadimitriou, C Razis, E Christodoulou, C Fountzilas, G Yannoukakos, D Konstantopoulou, I Fostira, F Producer: 20170630 In: Clinical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	High prevalence of BRCA1 founder mutations in Greek breast/ovarian families. [electronic resource] by Konstantopoulou, I Tsitlaidou, M Fostira, F Pertesi, M Stavropoulou, A-V Triantafyllidou, O Tsotra, E Tsiftsoglou, A P Tsionou, C Droufakou, S Dimitrakakis, C Fountzilas, G Yannoukakos, D Producer: 20140718 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Rare mutations in XRCC2 increase the risk of breast cancer. [electronic resource] by Park, D J Lesueur, F Nguyen-Dumont, T Pertesi, M Odefrey, F Hammet, F Neuhausen, S L John, E M Andrulis, I L Terry, M B Daly, M Buys, S Le Calvez-Kelm, F Lonie, A Pope, B J Tsimiklis, H Voegele, C Hilbers, F M Hoogerbrugge, N Barroso, A Osorio, A Giles, G G Devilee, P Benitez, J Hopper, J L Tavtigian, S V Goldgar, D E Southey, M C Producer: 20120531 In: American journal of human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Multigene testing of moderate-risk genes: be mindful of the missense. [electronic resource] by Young, E L Feng, B J Stark, A W Damiola, F Durand, G Forey, N Francy, T C Gammon, A Kohlmann, W K Kaphingst, K A McKay-Chopin, S Nguyen-Dumont, T Oliver, J Paquette, A M Pertesi, M Robinot, N Rosenthal, J S Vallee, M Voegele, C Hopper, J L Southey, M C Andrulis, I L John, E M Hashibe, M Gertz, J Le Calvez-Kelm, F Lesueur, F Goldgar, D E Tavtigian, S V Producer: 20171031 In: Journal of medical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)