343 related articles for article (PubMed ID: 12889647)
1. An ethical imperative: genetics education for physicians and patients.
Kegley JA
Med Law; 2003; 22(2):275-83. PubMed ID: 12889647
[TBL] [Abstract][Full Text] [Related]
2. Managing familial risk in genetic testing.
Taub S; Morin K; Spillman MA; Sade RM; Riddick FA;
Genet Test; 2004; 8(3):356-9. PubMed ID: 15727262
[TBL] [Abstract][Full Text] [Related]
3. Ethical considerations of genetic testing.
Fleming DA
J Clin Ethics; 2002; 13(4):316-23. PubMed ID: 12793324
[No Abstract] [Full Text] [Related]
4. The Human Genome Project and public perception: truth and consequences.
Pelias MZ; Markward NJ
Emory Law J; 2000; 49(3):837-58. PubMed ID: 12645564
[No Abstract] [Full Text] [Related]
5. Bioethics for clinicians: 14. Ethics and genetics in medicine.
Burgess MM; Laberge CM; Knoppers BM
CMAJ; 1998 May; 158(10):1309-13. PubMed ID: 9614824
[TBL] [Abstract][Full Text] [Related]
6. [First guidelines of the German Genetic Diagnostic Commission].
Tönnies H
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2011 Nov; 54(11):1145-6. PubMed ID: 22015785
[No Abstract] [Full Text] [Related]
7. [The limits of the physician's secrecy duty in risk situations. Special reference to genetics].
Gómez Rivero Mdel C
Rev Derecho Genoma Hum; 2007; (26):43-89. PubMed ID: 18201038
[TBL] [Abstract][Full Text] [Related]
8. Genetic testing and counseling: selected ethical issues.
Erlen JA
Orthop Nurs; 2006; 25(6):423-6. PubMed ID: 17130767
[TBL] [Abstract][Full Text] [Related]
9. Genetic privacy: the potential for genetic discrimination in insurance.
Jensen P
Law Rev; 1999 Apr; 29(2):347-69. PubMed ID: 12741371
[No Abstract] [Full Text] [Related]
10. 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]
11. Genetic secrets and the family: a response to Bell and Bennett.
Skene L
Med Law Rev; 2001; 9(2):162-9. PubMed ID: 12778931
[No Abstract] [Full Text] [Related]
12. Informed consent when taking genetic decisions.
Conti A; Delbon P; Sirignano A
Med Law; 2004; 23(2):337-53. PubMed ID: 15270473
[TBL] [Abstract][Full Text] [Related]
13. Genetic testing without consent: the implications of the new Human Tissue Act 2004.
Lucassen A; Kaye J
J Med Ethics; 2006 Dec; 32(12):690-2. PubMed ID: 17145906
[TBL] [Abstract][Full Text] [Related]
14. Safeguarding human genetic privacy.
Judicature; 2003; 86(5):224. PubMed ID: 15744895
[No Abstract] [Full Text] [Related]
15. Are guidelines for genetic testing of children necessary?
Fenwick A
Fam Cancer; 2010 Mar; 9(1):23-5. PubMed ID: 19685282
[TBL] [Abstract][Full Text] [Related]
16. [Guideline of the Gendiagnostik Kommission (GEKO) for genetic screening of consent incapable persons in accordance with 14 in connection with 23 Abs. 2 No. 1c GenDG. The 26 July 2011 version released and implemented 27 July 2011].
Gendiagnostik Kommission (GEKO)
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2011 Nov; 54(11):1257-61. PubMed ID: 22015799
[No Abstract] [Full Text] [Related]
17. Ethical issues raised by genetic testing with oligonucleotide microarrays.
Grody WW
Mol Biotechnol; 2003 Feb; 23(2):127-38. PubMed ID: 12632697
[TBL] [Abstract][Full Text] [Related]
18. Genetic information: a joint account?
Parker M; Lucassen AM
BMJ; 2004 Jul; 329(7458):165-7. PubMed ID: 15258076
[TBL] [Abstract][Full Text] [Related]
19. Predictive genetic testing in urology: ethical and social issues.
Mehlman MJ
World J Urol; 2004 Feb; 21(6):433-7. PubMed ID: 14691643
[TBL] [Abstract][Full Text] [Related]
20. Providing family guidance in rapidly shifting sand: informed consent for genetic testing.
Cohen J; Hoon A; Wilms Floet AM
Dev Med Child Neurol; 2013 Aug; 55(8):766-8. PubMed ID: 23398268
[No Abstract] [Full Text] [Related]
[Next] [New Search]
