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45 results on '"Courtney, Eliza"'

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1. Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival

3. Genetic counseling workforce diversity, inclusion, and capacity in Australia and New Zealand

4. Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum

5. The impact of coding germline variants on contralateral breast cancer risk and survival

6. Policy and process for returning raw genomic data to parents and young adult participants in a pediatric cancer precision medicine trial.

10. Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

11. The Global State of the Genetic Counseling Profession

14. Parents’ expectations, preferences, and recall of germline findings in a childhood cancer precision medicine trial

22. Missed diagnosis or misdiagnosis: Common pitfalls in genetic testing

23. Missed diagnosis or misdiagnosis: common pitfalls in genetic testing.

27. Investigation into the origins of an ancient BRCA1 founder mutation identified among Chinese families in Singapore

31. Identifying ataxia‐telangiectasia in cancer patients: Novel insights from an interesting case and review of literature.

32. Investigation into the origins of an ancient BRCA1 founder mutation identified among Chinese families in Singapore.

33. Evaluating empowerment in genetic counseling using patient‐reported outcomes.

35. The Global State of the Genetic Counseling Profession

36. Germline Pathogenic Variants in Homologous Recombination and DNA Repair Genes in an Asian Cohort of Young-Onset Colorectal Cancer

40. Clinical management of pheochromocytoma and paraganglioma in Singapore: missed opportunities for genetic testing

41. Evaluation of the relative effectiveness of the 2017 updated Manchester scoring system for predicting BRCA1/2 mutations in a Southeast Asian country.

42. Evaluation of the relative effectiveness of the 2017 updated Manchester scoring system for predicting BRCA1/2mutations in a Southeast Asian country

44. Protocol for a comprehensive prospective cohort study of trio-based whole-genome sequencing for underlying cancer predisposition in paediatric and adolescent patients newly diagnosed with cancer: the PREDICT study.

45. Functional analysis of clinical BARD1 germline variants.

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