| 期刊論文1. | 何建志、陳麗娟(20080700)。瑞士聯邦人類基因檢驗法中譯。法律與生命科學,6,45-57。 延伸查詢 | 2. | Romero, Stephanie、Rink, Britton、Biggio, Joseph R. Jr.、Saller, Devereux N. Jr.(2017)。Committee Opinion No. 690 Summary: Carrier Screening in the Age of Genomic Medicine。The American College of Obstetricians and Gynecologists,129(3),595-596。 | 3. | 何建志、呂千佩(20091000)。歐洲人類遺傳學會未成年人基因檢驗準則評述。法律與生命科學,3(4),35-45。 延伸查詢 | 4. | Borry, Pascal、Van Hellemondt, Rachel E.、Sprumont, Dominique、Jales, Camilla F. D.、Rial-Sebbag, Emmanuelle、Spranger, Tade M.、Curren, Liam、Kaye, Jane、Nys, Herman、Howard, Heidi(2012)。Legislation on Direct-to-Consumer Genetic Testing in Seven European Countries。European Journal of Human Genetics,20(7),715-721。 | 5. | 王美仁、林秀娟(20091000)。草擬臺灣基因檢測倫理指導綱領。法律與生命科學,3(4),1-21。 延伸查詢 | 6. | Gill, Jennifer、Obley, Adam J.、Prasad, Vinay(2018)。Direct-to-Consumer Genetic Testing: The Implications of the US FDA's First Marketing Authorization for BRCA Mutation Testing。JAMA,319(23),2377-2378。 | 7. | Mills, Rachel、Haga, Susanne B.(2014)。Genomic Counseling: Next Generation Counseling。Journal of Genetic Counseling,23(4),689-692。 | 8. | 李美欣(2017)。台灣遺傳諮詢現況及未來發展。台灣遺傳諮詢學會會刊,1(1)。 延伸查詢 | 9. | Gaff, Clara L.、Winship, Ingrid M.、Forrest, Susan M.、Hansen, David P.、Clark, Julian、Waring, Paul M.、South, Mike、Sinclair, Andrew H.(2017)。Preparing for Genomic Medicine: A Real World Demonstration of Health System Change。NPJ Genomic Medicine,2(16)。 | 10. | Patch, Christine、Middleton, Anna(2018)。Genetic Counselling in the Era of Genomic Medicine。British Medical Bulletin,126,27-36。 | 11. | Brett, Gemma R.、Wilkins, Ella J.、Creed, Emma T.、West, Kirsty、Jarmolowicz, Anna、Valente, Giulia M.、Prawer, Yael、Lynch, Sly、Macciocca, Ivan(2018)。Genetic Counseling in the Era of Genomics: What's All the Fuss about?。Journal of Genetic Counseling,27(5)。 | 12. | Kalia, Sarah S.、Adelman, Kathy、Bale, Sherri J.、Chung, Wendy K.、Eng, Christine、Evans, James P.、Herman, Gail E.、Hufnagel, Sophia B.、Klein, Teri E.、Korf, Bruce R.、McKelvey, Kent D.、Ormond, Kelly E.、Richards, C. Sue、Vlangos, Christopher N.、Watson, Michael、Martin, Christa L.、Miller, David T.(2017)。Recommendations for Reporting of Secondary Findings in Clinical Exome and Genome Sequencing, 2016 Update (ACMG SF v2.0): A Policy Statement of the American College of Medical Genetics and Genomics。Genetics in Medicine,19(2),249-255。 | 13. | Van der Hout, Sanne、Holtkamp, Kim C. A.、Henneman, Lidewij、De Wert, Guido、Dondorp, Wybo J.(2017)。Advantages of Expanded Universal Carrier Screening: What Is at Stake?。European Journal of Human Genetics,25(1),17-21。 | 圖書1. | 國民健康署。新興產前遺傳檢測指引及諮詢參考手冊電子書。 延伸查詢 | |