期刊論文1. | Wiesemann, C.、Ude-Koeller, S.、Sinnecker, G. H.、Thyen, U.(2010)。Ethical principles and recommendations for the medical management of differences of sex development (DSD)/intersex in children and adolescents。Eur J Pediatr,169(6),671-679。 ![](/gs32/thssjcncl/image/nclsfx.gif) ![new window](/gs32/images/newin.png) |
2. | Palacios-González, C.、Ishii, T.(2017)。Mitochondrial Replacement Techniques: Genetic Relatedness, Gender Implications, and Justice。Gender and the Genome,1(4),129-134。 ![](/gs32/thssjcncl/image/nclsfx.gif) ![new window](/gs32/images/newin.png) |
3. | 黃美智、林秀娟、陳祉伶、黃子容(20171000)。新興產前遺傳檢測之臨床運用及倫理考量。護理雜誌,64(5),5-10。 延伸查詢![new window](/gs32/images/newin.png) |
4. | 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。 ![](/gs32/thssjcncl/image/nclsfx.gif) ![new window](/gs32/images/newin.png) |
5. | 陳俞沛、林建智、林秀娟(20121000)。遺傳疾病病患隱私與親屬利益衝突之倫理法制探討。東吳法律學報,24(2),35-81。 延伸查詢![new window](/gs32/images/newin.png) |
6. | 林秀娟(20181100)。基因諮商的倫理與規範。月旦醫事法報告,25,72-82。 延伸查詢![new window](/gs32/images/newin.png) |
7. | Lee, I.-W.、Chou, Y.-Y.、Hsu, K.-F.(2011)。Complex chromosome rearrangement 46, XY, der (9) t (Y; 9)(q12; p23) in a girl with sex reversal and mental retardation。Urology,77(5),1213-1216。 ![](/gs32/thssjcncl/image/nclsfx.gif) ![new window](/gs32/images/newin.png) |
8. | Chen, S.-Y.、Lin, S.-J.、Tsai, L.-P.、Chou, Y.- Y.(2012)。Sex-reversed acampomelic campomelic dysplasia with a homozygous deletion mutation in SOX9 gene。Urology,79(4),908-911。 ![](/gs32/thssjcncl/image/nclsfx.gif) ![new window](/gs32/images/newin.png) |
9. | Lin, Y. M.、Chen, C. W.、Sun, H. S.(2000)。Y-chromosome microdeletion and its effect on reproductive decisions in Taiwanese patients presenting with non-obstructive azoospermia。Urology,56,1041-1046。 ![](/gs32/thssjcncl/image/nclsfx.gif) ![new window](/gs32/images/newin.png) |
10. | 陳雲絹、林秀娟、林佳霓、黃美智(20100900)。先天性腎上腺增生症患童父母之家庭經驗敘事。醫護科技期刊,12(3),199-211。 延伸查詢![new window](/gs32/images/newin.png) |
11. | Korf, B. R.、Berry, A. B.、Limson, M.(2014)。Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics。Genetics in medicine,16(11),804-809。 ![](/gs32/thssjcncl/image/nclsfx.gif) ![new window](/gs32/images/newin.png) |
12. | Hamilton, J. G.、Shuk, E.、Arniella, G.(2016)。Genetic testing awareness and attitudes among Latinos: exploring shared perceptions and gender-based differences。Public health genomics,19(1),34-46。 ![](/gs32/thssjcncl/image/nclsfx.gif) ![new window](/gs32/images/newin.png) |