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2. Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies. Issue 7 (1st July 2005)

3. Classification of BRCA1 missense variants of unknown clinical significance. Issue 2 (2nd February 2005)

4. Minimizing inequality in access to precision medicine in breast cancer by real-time population-based molecular analysis in the SCAN-B initiative. Issue 2 (17th January 2018)

5. Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies. Issue 11 (6th July 2006)