177 related articles for article (PubMed ID: 2949608)
1. Testing for the Huntington gene: a right to know, a right not to know, or a duty to know.
Shaw MW
Am J Med Genet; 1987 Feb; 26(2):243-6. PubMed ID: 2949608
[No Abstract] [Full Text] [Related]
2. Predictive testing for Huntington disease and the right not to know. Some ethical reflections.
de Wert G
Birth Defects Orig Artic Ser; 1992; 28(1):133-8. PubMed ID: 1340223
[No Abstract] [Full Text] [Related]
3. Presymptomatic testing for Huntington disease: is there a duty to test those under the age of eighteen years?
Sharpe NF
Am J Med Genet; 1993 Apr; 46(2):250-3. PubMed ID: 8053988
[No Abstract] [Full Text] [Related]
4. Informed consent and Huntington disease: a model for communication.
Sharpe NF
Am J Med Genet; 1994 Apr; 50(3):239-46. PubMed ID: 8042667
[TBL] [Abstract][Full Text] [Related]
5. Genetic jeopardy and the new clairvoyance.
Wexler NS
Prog Med Genet; 1985; 6():277-304. PubMed ID: 2941821
[No Abstract] [Full Text] [Related]
6. Presymptomatic testing for Huntington chorea: guidelines for moral and social accountability.
Smurl JF; Weaver DD
Am J Med Genet; 1987 Feb; 26(2):247-57. PubMed ID: 2949609
[TBL] [Abstract][Full Text] [Related]
7. Pitfalls in counseling for predictive testing in Huntington disease.
Demyttenaere K; Evers-Kiebooms G; Decruyenaere M
Birth Defects Orig Artic Ser; 1992; 28(1):105-11. PubMed ID: 1340218
[No Abstract] [Full Text] [Related]
8. The right not to know and preimplantation genetic diagnosis for Huntington's disease.
Asscher E; Koops BJ
J Med Ethics; 2010 Jan; 36(1):30-3. PubMed ID: 20026690
[TBL] [Abstract][Full Text] [Related]
9. Ensuring consumer safety. Predictive testing for Huntington disease: response to Dr. Seymour Kessler, "Reinventing the wheel".
Chapman MA
Am J Med Genet; 1993 Mar; 45(6):698-710. PubMed ID: 8456848
[No Abstract] [Full Text] [Related]
10. The perils of knowing.
Klotzko AJ
Nurs Times; 1998 Oct 28-Nov 3; 94(43):32-3. PubMed ID: 9887833
[No Abstract] [Full Text] [Related]
11. Attitudes of persons at risk for Huntington disease toward predictive testing.
Kessler S; Field T; Worth L; Mosbarger H
Am J Med Genet; 1987 Feb; 26(2):259-70. PubMed ID: 2949610
[TBL] [Abstract][Full Text] [Related]
12. Medical ethics. A tough line on genetic screening.
Marshall E
Science; 1993 Nov; 262(5136):984-5. PubMed ID: 8235637
[No Abstract] [Full Text] [Related]
13. Genetic markers and the majority's right not to know.
Appel J; Friedman JH
Mov Disord; 2004 Jan; 19(1):113-4. PubMed ID: 14743372
[No Abstract] [Full Text] [Related]
14. Comment: limiting toxic information.
Howe EG
J Clin Ethics; 2001; 12(2):143-9. PubMed ID: 11642066
[No Abstract] [Full Text] [Related]
15. DNA testing and genetic counseling: truth or consequences.
Reynolds NC; Lebel RR; Hamsher Kde S; Blackwell B; Elejalde BR; Winter GR
Wis Med J; 1994 Feb; 93(2):51-4. PubMed ID: 8191778
[TBL] [Abstract][Full Text] [Related]
16. Psychological aspects of genetic counseling: a legal perspective.
Sharpe NF
Am J Med Genet; 1994 Apr; 50(3):234-8. PubMed ID: 8042666
[TBL] [Abstract][Full Text] [Related]
17. Genetic testing and mental health: the model of Huntington disease.
Williams JK; Schutte DL
Online J Issues Nurs; 2000; 5(3):3. PubMed ID: 11380269
[TBL] [Abstract][Full Text] [Related]
18. [Psychotic syndrome in chorea Huntington].
Känzig S; Eichorn M
Psychiatr Prax; 2003 Jul; 30(5):286-7. PubMed ID: 12947934
[No Abstract] [Full Text] [Related]
19. AIDS: the rights of patients.
Charrel J; Larher MP; Manuel C; Enel P; Reviron D; San Marco JL
AIDS Public Policy J; 1991; 6(1):41-5. PubMed ID: 11651159
[No Abstract] [Full Text] [Related]
20. Patients' rights to laboratory data: trinucleotide repeat length in Huntington disease.
Burgess MM; Hayden MR
Am J Med Genet; 1996 Mar; 62(1):6-9. PubMed ID: 8779327
[No Abstract] [Full Text] [Related]
[Next] [New Search]