1,025 results on '"Borry, Pascal"'
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2. 23 X and Y
3. Table of Contents
4. Title Page, Copyright
5. Cover
6. Recommended Literature
7. About the Authors
8. 19 Personalizing Medicine to Fit Your Genetic Profile
9. 16 Mudbloods
10. 21 Consumer Genomics
11. 18 The Godfather
12. 22 Genes and Patents
13. 14 Genome Hackers
14. 20 Gene Therapy, a Medicine?
15. 15 A Neanderthal in All of Us?
16. 17 My Olympic DNA
17. 13 HELP! The Government Has My DNA!
18. 11 Everyone’s Genome Investigated
19. 12 Finding out More Than You Would Want to Know
20. 10 As Long as it Stays in the Family
21. 3 A Gene, a Genome, and Then What?
22. 9 Designer Babies
23. 8 New Test Tracks for Fetus DNA
24. 7 We Are All Carriers
25. 6 Give Me Back My DNA!
26. 5 Angelina Jolie’s Choice
27. 1 The Genome: The Cookbook of Life
28. 4 Genetic Disorders
29. 2 Reading Genomes
30. Introduction
31. Implementation of Electronic Informed Consent in Biomedical Research and Stakeholders’ Perspectives: Systematic Review
32. Polygenic embryo screening: quo vadis?
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. Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography
38. Safeguarding Users of Consumer Mental Health Apps in Research and Product Improvement Studies: an Interview Study
39. Correction: Clinician perspectives on policy approaches to genetic risk disclosure in families
40. Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screening
41. Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores
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. “Are we not going too far?“: Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionals
46. Attitudes of professional stakeholders towards implementation of reproductive genetic carrier screening: a systematic review
47. Expanded Non-invasive Prenatal Testing (NIPT): Can the Child’s Right to an Open Future Help Set the Scope?
48. Disclosure of genetic risk in the family: A survey of the Flemish general population
49. Toward better governance of human genomic data
50. Knowledge, attitudes and preferences regarding reproductive genetic carrier screening among reproductive-aged men and women in Flanders (Belgium)
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