929 results on '"Borry, Pascal"'
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2. Polygenic embryo screening: quo vadis?
3. Implementation of Electronic Informed Consent in Biomedical Research and Stakeholders’ Perspectives: Systematic Review
4. 23 X and Y
5. Table of Contents
6. Title Page, Copyright
7. Cover
8. Recommended Literature
9. About the Authors
10. 19 Personalizing Medicine to Fit Your Genetic Profile
11. 16 Mudbloods
12. 21 Consumer Genomics
13. 18 The Godfather
14. 22 Genes and Patents
15. 14 Genome Hackers
16. 20 Gene Therapy, a Medicine?
17. 15 A Neanderthal in All of Us?
18. 17 My Olympic DNA
19. 13 HELP! The Government Has My DNA!
20. 11 Everyone’s Genome Investigated
21. 12 Finding out More Than You Would Want to Know
22. 10 As Long as it Stays in the Family
23. 3 A Gene, a Genome, and Then What?
24. 9 Designer Babies
25. 8 New Test Tracks for Fetus DNA
26. 7 We Are All Carriers
27. 6 Give Me Back My DNA!
28. 5 Angelina Jolie’s Choice
29. 1 The Genome: The Cookbook of Life
30. 4 Genetic Disorders
31. 2 Reading Genomes
32. Introduction
33. Clinician perspectives on policy approaches to genetic risk disclosure in families
34. Contact investigation in multidrug-resistant tuberculosis: ethical challenges
35. Exploring attitudes and experiences with reproductive genetic carrier screening among couples seeking medically assisted reproduction: a longitudinal survey study
36. Reconciling the biomedical data commons and the GDPR: three lessons from the EUCAN ELSI collaboratory
37. Safeguarding Users of Consumer Mental Health Apps in Research and Product Improvement Studies: an Interview Study
38. Correction: Clinician perspectives on policy approaches to genetic risk disclosure in families
39. Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography
40. Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores
41. Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screening
42. Opt-in or out? Public perspectives on forensic DNA kinship investigations within the Dutch-speaking community
43. Informing a European guidance framework on electronic informed consent in clinical research: a qualitative study
44. Can I use the placebo effect to treat injured or Ill athletes?
45. Attitudes of professional stakeholders towards implementation of reproductive genetic carrier screening: a systematic review
46. “Are we not going too far?“: Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionals
47. Expanded Non-invasive Prenatal Testing (NIPT): Can the Child’s Right to an Open Future Help Set the Scope?
48. Toward better governance of human genomic data
49. Disclosure of genetic risk in the family: A survey of the Flemish general population
50. Knowledge, attitudes and preferences regarding reproductive genetic carrier screening among reproductive-aged men and women in Flanders (Belgium)
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