A. Arffman

A Finnish BRCA1 exon 12 4216‐2nt A to G splice acceptor site mutation causes aberrant splicing and frameshift, leading to protein truncation

A. Mannermaa, J. Hartikainen, M. Pirskanen, 2000, Human mutation.

Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families

A. Mannermaa, V. Kosma, V. Kataja, 2007, Clinical genetics.

An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found.

D. Easton, A. Antoniou, A. Dunning, 2005, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.