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2. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Issue 1 (December 2016)

3. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS. Issue 12 (5th September 2016)

4. Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer. Issue 11 (31st January 2018)