These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
154 related articles for article (PubMed ID: 11657302)
1. Advances in genetics: issues for US racial and ethnic minorities: an Asian American and Pacific Islander perspective. Lin-Fu JS Community Genet; 1998; 1(3):124-9. PubMed ID: 11657302 [No Abstract] [Full Text] [Related]
2. A national dialogue on genetics and minority issues. Mittman IS; Secundy MG Community Genet; 1998; 1(3):190-200. PubMed ID: 11657309 [No Abstract] [Full Text] [Related]
3. Ethical principles and cultural integrity in health care delivery: Asian ethnocultural perspectives in genetic services. Wang V; Marsh FH J Genet Couns; 1992 Mar; 1(1):81-92. PubMed ID: 11651282 [No Abstract] [Full Text] [Related]
4. Setting research priorities: human germ-line gene therapy in perspective. Blank RH Politics Life Sci; 1994 Aug; 13(2):221-2. PubMed ID: 11654633 [No Abstract] [Full Text] [Related]
5. What are society's interests in human genetics and reproductive technologies? Fletcher JC Law Med Health Care; 1988; 16(1-2):131-7. PubMed ID: 11659073 [No Abstract] [Full Text] [Related]
6. The difficulties of recruiting minorities to studies of ethics and values in genetics. Wertz DC Community Genet; 1998; 1(3):175-9. PubMed ID: 11657307 [No Abstract] [Full Text] [Related]
7. Science and social harm: genetic research into crime and violence. Wasserman D Rep Inst Philos Public Policy; 1995; 15(1):14-9. PubMed ID: 11652935 [No Abstract] [Full Text] [Related]
9. Eugenics and the new genetics in Britain: examining contemporary professionals' accounts. Kerr A; Cunningham-Burley S; Amos A Sci Technol Human Values; 1998; 23(2):175-98. PubMed ID: 11656684 [No Abstract] [Full Text] [Related]
10. Access to reproductive genetic services for low-income women and women of color. Nsiah-Jefferson L Fetal Diagn Ther; 1993 Apr; 8(Suppl. 1):107-27. PubMed ID: 11653012 [TBL] [Abstract][Full Text] [Related]
11. The Human Genome Project: a challenge to the human rights framework. Iles AT Harv Hum Rights J; 1996; 9():27-60. PubMed ID: 11660498 [No Abstract] [Full Text] [Related]
12. Proposed recommendations of the Task Force on Genetic Testing; notice of meeting and request for comment. U.S. National Institutes of Health Fed Regist; 1997 Jan; 62(20):4539-47. PubMed ID: 11660342 [No Abstract] [Full Text] [Related]
13. Map, myth, or medium of redemption: how do we interpret the Human Genome Project? Lysaught MT Second Opin; 1994 Apr; 19(4):76-84. PubMed ID: 11645259 [No Abstract] [Full Text] [Related]
14. Legal and ethical issues in newborn screening. Bowman JE Pediatrics; 1989 May; 83(5 part 2):894-6. PubMed ID: 11651963 [No Abstract] [Full Text] [Related]
15. Where in the world are we going with the new genetics? Fletcher JC J Contemp Health Law Policy; 1989; 5():33-51. PubMed ID: 11645622 [No Abstract] [Full Text] [Related]
16. Ethics of prediction: genetic risk and the physician-patient relationship. Juengst ET Genome Sci Technol; 1995; 1(1):21-36. PubMed ID: 11660453 [No Abstract] [Full Text] [Related]
17. An unsuitable case for treatment. Vines G New Sci; 1995 Sep; 147(1994):37-9. PubMed ID: 11656470 [No Abstract] [Full Text] [Related]
19. The UK's policy on genetic testing services supplied direct to the public -- two spheres and two tiers. Holtzman NA Community Genet; 1998; 1(1):49-52. PubMed ID: 11660582 [No Abstract] [Full Text] [Related]
20. The Human Genome Diversity Project: ethical problems and solutions. Resnik DB Politics Life Sci; 1999 Mar; 18(1):15-23. PubMed ID: 11660815 [No Abstract] [Full Text] [Related] [Next] [New Search]