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1
The genetic testing of children. Working Party of the Clinical Genetics Society (UK).儿童基因检测。（英国）临床遗传学协会工作小组
J Med Genet. 1994 Oct;31(10):785-97. doi: 10.1136/jmg.31.10.785.
2
Testing children for genetic predispositions: is it in their best interest?
J Law Med Ethics. 1995 Winter;23(4):331-44. doi: 10.1111/j.1748-720x.1995.tb01375.x.
3
GIG response to the UK Clinical Genetics Society report "The genetic testing of children".基因检测行业组织（GIG）对英国临床遗传学协会报告《儿童基因检测》的回应。
J Med Genet. 1995 Jun;32(6):490-1. doi: 10.1136/jmg.32.6.490.
4
Laboratory policies and practices for the genetic testing of children: a survey of the Helix network.儿童基因检测的实验室政策与实践：对Helix网络的一项调查
Am J Hum Genet. 1997 Nov;61(5):1163-8. doi: 10.1086/301593.
5
Genetic testing for hereditary disease: attending to relational responsibility.遗传性疾病的基因检测：关注关系责任。
J Clin Ethics. 2001 Winter;12(4):361-72.
6
The genetic testing of children.儿童的基因检测
J Med Genet. 1995 Jun;32(6):492. doi: 10.1136/jmg.32.6.492.
7
Genetic testing for children and adolescents. Who decides?儿童和青少年的基因检测。由谁来决定？
JAMA. 1994 Sep 21;272(11):875-81.
8
The genetic revolution and the physician's duty of confidentiality. The role of the old Hippocratic virtues in the regulation of the new genetic intimacy.基因革命与医生的保密义务。古老的希波克拉底誓言在规范新型基因隐私方面的作用。
J Leg Med. 1997 Dec;18(4):401-41. doi: 10.1080/01947649709511044.
9
Ethical considerations in the social context of Huntington disease.亨廷顿舞蹈症社会背景下的伦理考量
Dis Markers. 1992 Jul-Aug;10(4):171-83; discussion 211-28.
10
Genetic testing in children.儿童基因检测
J Med Philos. 1997 Jun;22(3):233-51. doi: 10.1093/jmp/22.3.233.

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1
Predicting age of onset and progression of disease in late-onset genetic neurodegenerative diseases: An ethics review and research agenda.预测晚发性遗传神经退行性疾病的发病年龄和疾病进展：伦理审查和研究议程。
Eur J Hum Genet. 2024 Nov;32(11):1361-1370. doi: 10.1038/s41431-024-01688-7. Epub 2024 Sep 24.
2
Can Genomics Remove Uncertainty from Adoption? Social Workers' and Medical Advisors' Accounts of Genetic Testing.基因组学能否消除采用过程中的不确定性？社会工作者和医学顾问对基因检测的看法。
Br J Soc Work. 2021 Feb 24;52(2):719-737. doi: 10.1093/bjsw/bcab017. eCollection 2022 Mar.
3
'We Should View Him as an Individual': The Role of the Child's Future Autonomy in Shared Decision-Making About Unsolicited Findings in Pediatric Exome Sequencing.“我们应该将他视为一个个体”：儿科外显子组测序中未征求意见的发现的共享决策中儿童未来自主性的作用。
Health Care Anal. 2021 Sep;29(3):249-261. doi: 10.1007/s10728-020-00425-7. Epub 2021 Jan 2.
4
Citizens under the umbrella: citizenship projects and the development of genetic umbrella organizations in the USA and the UK.保护伞下的公民：公民身份项目与美国和英国基因保护伞组织的发展
New Genet Soc. 2020 Mar 6;39(2):148-172. doi: 10.1080/14636778.2019.1693889. eCollection 2020.
5
Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.新生儿测序研究中的伦理问题：以 BabySeq 为例。
Pediatrics. 2019 Dec;144(6). doi: 10.1542/peds.2019-1031. Epub 2019 Nov 12.
6
Rethinking the "open future" argument against predictive genetic testing of children.重新思考反对对儿童进行预测性基因检测的“开放未来”论点。
Genet Med. 2019 Oct;21(10):2190-2198. doi: 10.1038/s41436-019-0483-4. Epub 2019 Mar 21.
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"They Just Want to Know" - Genetic Health Professionals' Beliefs About Why Parents Want to Know their Child's Carrier Status.“他们只是想知道”——遗传健康专家对父母想了解孩子携带者状态原因的看法。
J Genet Couns. 2017 Dec;26(6):1314-1323. doi: 10.1007/s10897-017-0070-2. Epub 2017 Feb 4.
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Predictive Genetic Testing of Children for Adult-Onset Conditions: Negotiating Requests with Parents.对儿童进行成人发病疾病的预测性基因检测：与家长协商检测请求
J Genet Couns. 2017 Apr;26(2):244-250. doi: 10.1007/s10897-016-0018-y. Epub 2016 Sep 28.
9
Why Do Parents Want to Know their Child's Carrier Status? A Qualitative Study.为何父母想知道孩子的携带者状态？一项定性研究。
J Genet Couns. 2016 Dec;25(6):1257-1266. doi: 10.1007/s10897-016-9964-7. Epub 2016 May 19.
10
Impact of presymptomatic genetic testing on young adults: a systematic review.症状前基因检测对年轻人的影响：一项系统综述
Eur J Hum Genet. 2016 Apr;24(4):496-503. doi: 10.1038/ejhg.2015.153. Epub 2015 Jul 15.

本文引用的文献

1
Research samples from families with genetic diseases: a proposed code of conduct.来自患有遗传疾病家庭的研究样本：一项拟议的行为准则。
BMJ. 1993 May 22;306(6889):1391-4. doi: 10.1136/bmj.306.6889.1391.
2
Uptake of cystic fibrosis testing in primary care: supply push or demand pull?基层医疗中囊性纤维化检测的应用：供应推动还是需求拉动？
BMJ. 1993 Jun 12;306(6892):1584-6. doi: 10.1136/bmj.306.6892.1584.
3
Adoption, genetic disease, and DNA.收养、遗传疾病与DNA。
Arch Dis Child. 1993 Oct;69(4):411-3. doi: 10.1136/adc.69.4.411.
4
Insurance and genetic testing.保险与基因检测。
Lancet. 1993 Jan 23;341(8839):224-7. doi: 10.1016/0140-6736(93)90080-z.
5
Presymptomatic testing for Huntington disease: is there a duty to test those under the age of eighteen years?亨廷顿病的症状前检测：是否有义务对18岁以下的人进行检测？
Am J Med Genet. 1993 Apr 15;46(2):250-3. doi: 10.1002/ajmg.1320460232.
6
A private view of heterozygosity: eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in Montreal.杂合性的个体观察：对在蒙特利尔高中筛查中检测出的泰-萨克斯基因携带者的八年随访研究
Am J Med Genet. 1984 Aug;18(4):769-78. doi: 10.1002/ajmg.1320180424.
7
A genetic register for Huntington's chorea in South Wales.南威尔士亨廷顿舞蹈症基因登记册。
J Med Genet. 1982 Aug;19(4):241-5. doi: 10.1136/jmg.19.4.241.
8
Psychological consequences of neonatal screening for alpha 1-antitrypsin deficiency. Parental reactions to the first news of their infants' deficiency.α1-抗胰蛋白酶缺乏症新生儿筛查的心理影响。父母对其婴儿缺乏该症的首个消息的反应。
Acta Paediatr Scand. 1985 Sep;74(5):787-93. doi: 10.1111/j.1651-2227.1985.tb10032.x.
9
Invited essay on the psychological aspects of genetic counseling. V. Preselection: a family coping strategy in Huntington disease.
Am J Med Genet. 1988 Nov;31(3):617-21. doi: 10.1002/ajmg.1320310316.
10
Ethics of predictive testing for Huntington's chorea: the need for more information.亨廷顿舞蹈症预测性检测的伦理问题：需要更多信息。
Br Med J (Clin Res Ed). 1986 Jul 26;293(6541):249-51. doi: 10.1136/bmj.293.6541.249.

The genetic testing of children. Working Party of the Clinical Genetics Society (UK).

作者信息

Clarke A

出版信息

J Med Genet. 1994 Oct;31(10):785-97. doi: 10.1136/jmg.31.10.785.

DOI:10.1136/jmg.31.10.785
PMID:7837256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1050126/
Abstract
摘要