| 期刊論文| 1. | 李崇僖(20070800)。生物科技專利族群化之社會影響與應有規範。月旦法學，147，224-242。 延伸查詢 | | 2. | Coleman, Doriane Lambelet(2007)。The Legal Ethics of Pediatric Research。Duke Law Journal，57，517。  | | 3. | Food and Drug Administration(1993)。Guidelines for the study and evaluation of gender differences in the clinical evaluation of drugs。Fed Register，58(139)，39406-39416。 | | 4. | Lynch, Holly Fernandez(2007)。Give Them What They Want? The Permissibility of Pediatric Placebo-controlled Trials under the Best Pharmaceuticals for Children Act。Annals of Health Law，16。 | | 5. | National Institutes of Health(1994)。NIH Guidelines on the Inclusion of Women and Minorities as Subjects in Clinical Research。Fed Register，59，14508-14513。 | | 6. | 李崇僖(20070900)。原住民基因研究之倫理課題與規範初探。國立臺灣大學法學論叢，36(3)，465-518。 延伸查詢 | 圖書| 1. | Reverby, Susan(2000)。Tuskegee's Truths: Rethinking the Tuskegee Syphilis Study。Chapel Hill：University of North Carolina。 | | 2. | Murphy, Timothy(2004)。Case Studies in Biomedical Research Ethics。MIT Press。 | 單篇論文| 1. | Collins, Francis(2001)。Implications of the Human Genome Project。 | | 2. | National Institutes of Health(1998)。NIH Policy and Guidelines on the Inclusion of Children as Participants in Research Involving Human Subjects。 | |