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42. Beyond the genome: the ethics of DNA testing. Fackelmann KA Sci News; 1994 Nov; 146(19):298-9. PubMed ID: 11659981 [No Abstract] [Full Text] [Related]
43. Towards a reconstruction of the "genetic family": new principles? Knoppers BM Int Dig Health Legis; 1998; 49(1):241-53. PubMed ID: 11658002 [No Abstract] [Full Text] [Related]
44. Information(al) matters: bioethics and the boundaries of the public and the private. Parker LS Soc Philos Policy; 2002; 19(2):83-112. PubMed ID: 12678083 [No Abstract] [Full Text] [Related]
45. Ethical issues in molecular screening for heterozygous familial hypercholesterolemia: the complexity of dealing with genetic susceptibility to coronary artery disease. Gaudet D; Gagné C; Perron P; Couture P; Tonstad S Community Genet; 1999; 2(1):2-8. PubMed ID: 11658106 [No Abstract] [Full Text] [Related]
46. The impact of prenatal genetic testing on quality of life in women. Gates EA Fetal Diagn Ther; 1993 Apr; 8(Suppl. 1):226-43. PubMed ID: 11653021 [No Abstract] [Full Text] [Related]
47. Genetic screening for breast cancer susceptibility: a Torah perspective. Mosenkis A J Halacha Contemporary Society; 1997; No. 34():5-26. PubMed ID: 11660426 [No Abstract] [Full Text] [Related]
48. Is knowledge always good? King D Genethics News; 1996; No. 12():6-7. PubMed ID: 11655116 [No Abstract] [Full Text] [Related]
49. A clinical approach to legal and ethical problems in human genetics. Elsas LJ Emory Law J; 1990; 39(3):811-53. PubMed ID: 11653909 [No Abstract] [Full Text] [Related]
50. Genetics and the interpersonal elaboration of ethics. Parker M Theor Med Bioeth; 2001 Sep; 22(5):451-9. PubMed ID: 11808679 [TBL] [Abstract][Full Text] [Related]
55. Genetic links, family ties, and social bonds: rights and responsibilities in the face of genetic knowledge. Rhodes R J Med Philos; 1998 Feb; 23(1):10-30. PubMed ID: 9555632 [TBL] [Abstract][Full Text] [Related]
56. Presymptomatic and predisposition genetic testing: ethical and social considerations. Bove CM; Fry ST; MacDonald DJ Semin Oncol Nurs; 1997 May; 13(2):135-40. PubMed ID: 9114482 [TBL] [Abstract][Full Text] [Related]
57. Testing for HD in twins. Reich E; Zanko A; Heimler A J Genet Couns; 1996 Mar; 5(1):47-51. PubMed ID: 11657408 [No Abstract] [Full Text] [Related]
58. Diffusion of information about genetic risk within families. Ayme S; Macquart-Moulin G; Julian-Reynier C; Chabal F; Giraud F Neuromuscul Disord; 1993; 3(5-6):571-4. PubMed ID: 11660032 [TBL] [Abstract][Full Text] [Related]
59. Generic consistency in the reproductive enterprise: ethical and legal implications for exclusion testing for Huntington's disease. Beyleveld D; Quarrell O; Toddington S Med Law Int; 1998; 3(2-3):135-58. PubMed ID: 11657592 [No Abstract] [Full Text] [Related]
60. The right to genetic information: some reflections on Dutch developments. Van Leeuwen E; Hertogh C J Med Philos; 1992 Aug; 17(4):381-93. PubMed ID: 1431657 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]