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2. Primary constitutional MLH1 epimutations: a focal epigenetic event. Issue 8 (16th October 2018)

3. Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants. Issue 1 (17th October 2016)

4. A regional population‐based hereditary breast cancer screening tool in Italy: First 5‐year results. (11th February 2020)

6. Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion. Issue 11 (16th September 2011)

7. Definition and management of colorectal polyposis not associated with APC/MUTYH germline pathogenic variants: AIFEG consensus statement. Issue 4 (April 2021)

8. BRCA-Associated Ovarian Cancer: From Molecular Genetics to Risk Management. (22nd July 2014)