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3. American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility. American Society of Clinical Oncology J Clin Oncol; 2003 Jun; 21(12):2397-406. PubMed ID: 12692171 [TBL] [Abstract][Full Text] [Related]
5. Promoting safe and effective genetic testing in the United States: Final Report of the Task Force on Genetic Testing. Harper PS Community Genet; 1998; 1(2):91-2. PubMed ID: 11657633 [No Abstract] [Full Text] [Related]
6. Genetic health care services, present and near future in Japan. Matsuda I Eubios J Asian Int Bioeth; 2003 Mar; 13(2):57-9. PubMed ID: 17117541 [TBL] [Abstract][Full Text] [Related]
7. Participation in pedigree studies and the risk of impeded access to health insurance. Kass NE IRB; 1993; 15(5):7-10. PubMed ID: 11659704 [No Abstract] [Full Text] [Related]
8. A conceptual framework for genetic policy: comparing the medical, public health, and fundamental rights models. Andrews LB Wash Univ Law Q; 2001; 79(152):221-85. PubMed ID: 16211786 [No Abstract] [Full Text] [Related]
9. Genetic testing, genetic medicine, and managed care. Rothstein MA; Hoffman S Wake Forest Law Rev; 1999; 34(3):849-88. PubMed ID: 12664926 [TBL] [Abstract][Full Text] [Related]
10. Genetic testing, access to genetic data and discrimination: conceptual legislative models. Brown B Suffolk Univ Law Rev; 1993; 27(4):1573-92. PubMed ID: 11657048 [No Abstract] [Full Text] [Related]
12. 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]
14. The link between providers and patients: how laboratories can ensure quality results with genetic testing. Quillin JM; Jackson-Cook C; Bodurtha J Clin Leadersh Manag Rev; 2003; 17(6):351-7. PubMed ID: 14692080 [TBL] [Abstract][Full Text] [Related]
15. Sharing scientific data II: normative issues. Weil V; Hollander R IRB; 1990; 12(2):7-8. PubMed ID: 11650369 [No Abstract] [Full Text] [Related]
16. [Ethical aspects. Confidentiality and informed consent]. Lisker R Gac Med Mex; 1997; 133 Suppl 1():75-7. PubMed ID: 9504106 [No Abstract] [Full Text] [Related]
17. Presentation on ethical issues associated with in utero gene therapy. Fletcher JC Hum Gene Ther; 1997 Jun; 8(9):1159-62. PubMed ID: 11644955 [No Abstract] [Full Text] [Related]
18. Part I: what is the requirement for data sharing? de Wolf VA; Sieber JE; Steel PM; Zarate AO IRB; 2005; 27(6):12-6. PubMed ID: 16425480 [No Abstract] [Full Text] [Related]
19. Quality assurance questionnaire for professionals fails to improve the quality of informed consent. Lavori PW; Wilt TJ; Sugarman J Clin Trials; 2007; 4(6):638-49. PubMed ID: 18042573 [TBL] [Abstract][Full Text] [Related]
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