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題名:基因諮商的倫理與規範
書刊名:月旦醫事法報告
作者:林秀娟
作者(外文):Lin, Shio-jean
出版日期:2018
卷期:25
頁次:頁72-82
主題關鍵詞:倫理規範基因諮商基因體醫學遺傳諮詢Ethical principleGenetic counselingGenomic medicineGenomic counseling
原始連結:連回原系統網址new window
相關次數:
  • 被引用次數被引用次數:期刊(1) 博士論文(0) 專書(0) 專書論文(0)
  • 排除自我引用排除自我引用:0
  • 共同引用共同引用:7
  • 點閱點閱:2
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。new window  延伸查詢new window
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。  new window
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。new window  延伸查詢new window
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。  new window
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。new window  延伸查詢new window
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。  new window
7.Mills, Rachel、Haga, Susanne B.(2014)。Genomic Counseling: Next Generation Counseling。Journal of Genetic Counseling,23(4),689-692。  new window
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new window
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)。  new window
10.Patch, Christine、Middleton, Anna(2018)。Genetic Counselling in the Era of Genomic Medicine。British Medical Bulletin,126,27-36。  new window
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)。  new window
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。  new window
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。  new window
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new window
 
 
 
 
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