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1. Brief family history questionnaire to screen for Lynch syndrome in women with newly diagnosed non-serous, non-mucinous ovarian cancers. Issue 7 (10th January 2022)

2. Candidate DNA repair susceptibility genes identified by exome sequencing in high-risk pancreatic cancer. Issue 2 (28th January 2016)

3. Comparison of Practice Guidelines, BRCAPRO, and Genetic Counselor Estimates to Identify Germline BRCA1 and BRCA2 Mutations in Pancreatic Cancer. Issue 4 (13th February 2018)

4. DNA Mismatch Repair Status Predicts Need for Future Colorectal Surgery for Metachronous Neoplasms in Young Individuals Undergoing Colorectal Cancer Resection. Issue 7 (July 2015)

5. Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study. Issue 4 (24th June 2020)

6. Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium. (February 2016)

7. Genetic testing for Lynch syndrome in the province of Ontario. Issue 11 (28th March 2016)

8. Lack of evidence for germline RNF43 mutations in patients with serrated polyposis syndrome from a large multinational study. Issue 6 (31st August 2016)

9. Maximizing cancer prevention through genetic navigation for Lynch syndrome detection in women with newly diagnosed endometrial and nonserous/nonmucinous epithelial ovarian cancer. Issue 17 (13th May 2021)

10. Overall Survival and Clinical Characteristics of BRCA‐Associated Cholangiocarcinoma: A Multicenter Retrospective Study. (9th May 2017)