21 results on '"Avard, Denise"'
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2. To disclose, or not to disclose? Context matters
3. Public views on participating in newborn screening using genome sequencing
4. Emerging issues in paediatric health research consent forms in Canada: working towards best practices
5. Exploring resources for intrafamilial communication of cancer genetic risk: we still need to talk
6. Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider
7. Recruiting Terminally Ill Patients into Non-Therapeutic Oncology Studies: views of Health Professionals
8. Personalized medicine and access to health care: potential for inequitable access?
9. Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?
10. Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening
11. The expansion of newborn screening: is reproductive benefit an appropriate pursuit?
12. Health-related direct-to-consumer genetic testing: a review of companies’ policies with regard to genetic testing in minors
13. Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information
14. Genomic medicine: considerations for health professionals and the public
15. Direct-to-consumer genome scanning services. Also for children?
16. Newborn Blood Spot Screening in Four Countries: Stakeholder Involvement
17. Improved Understanding of Genetic and Genomic Influences on Drug Disposition and Action
18. Newborn Screening by Tandem Mass Spectrometry
19. Variability in the storage and use of newborn dried bloodspots in Canada: is it time for national standards?
20. Ethics, industry and 'animal farm'
21. Children and incompetent adults in genetic research: consent and safeguards
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