• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Guidelines for genetic testing. The Japan Society of Human Genetics, Council Committee of Ethics.

作者信息

Matsuda I, Niikawa N, Sato K, Suzumori K, Fukushima Y, Fujiki N, Kanazawa I, Nakamura Y, Yonemoto S, Nakagome Y

出版信息

J Hum Genet. 2001;46(3):163-5. doi: 10.1007/s100380170107.

DOI:10.1007/s100380170107
PMID:11310587
Abstract
摘要

相似文献

1
Guidelines for genetic testing. The Japan Society of Human Genetics, Council Committee of Ethics.
J Hum Genet. 2001;46(3):163-5. doi: 10.1007/s100380170107.
2
Ethical aspects of medical genetics. A proposal for guidelines in genetic counseling, prenatal diagnosis and screening.医学遗传学的伦理问题。遗传咨询、产前诊断和筛查指南建议。
Clin Genet. 1985 Feb;27(2):199-205.
3
[Ethical aspects of programs for genetic screening premarital diagnosis and prenatal diagnosis of hereditary diseases].
Rev Invest Clin. 1980 Jan-Mar;32(1):1-5.
4
Medical-ethical guidelines for genetic investigations in humans.
Schweiz Med Wochenschr. 1994 Jun 4;124(22):974-9.
5
A clinical approach to legal and ethical problems in human genetics.人类遗传学中法律与伦理问题的临床处理方法。
Emory Law J. 1990 Summer;39(3):811-53.
6
Getting along with the genetic genie.与基因精灵和谐共处。
Leg Aspects Med Pract. 1979 Mar;7(3):37-41.
7
[Prenatal diagnosis--ethical aspects. Guidelines from the Ethics Committee of the Medical Society].[产前诊断——伦理方面。医学协会伦理委员会指南]
Lakartidningen. 1993 Jun 9;90(23):2232-6.
8
Ethical aspects of medical genetics. A proposal for guidelines in genetic counseling, prenatal diagnosis and screening.医学遗传学的伦理问题。关于遗传咨询、产前诊断和筛查指南的建议。
Prog Clin Biol Res. 1985;177:511-23.
9
Ethical issues in clinical genetics.临床遗传学中的伦理问题。
Prog Clin Biol Res. 1989;306:3-11.
10
Norms and standards of practice in genetic counselling.
Health Law J. 1995;3:153-74.

引用本文的文献

1
Mutational analysis in familial Alzheimer's disease of Han Chinese in Taiwan with a predominant mutation PSEN1 p.Met146Ile.台湾汉族家族性阿尔茨海默病中主要突变 PSEN1 p.Met146Ile 的突变分析。
Sci Rep. 2020 Nov 13;10(1):19769. doi: 10.1038/s41598-020-76794-9.
2
"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.
3
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.
4
Current status of preimplantation genetic diagnosis in Japan.日本胚胎植入前遗传学诊断的现状
Bioinformation. 2015 May 28;11(5):254-60. doi: 10.6026/97320630011254. eCollection 2015.
5
"Both Sides of the Wheelchair": The Views of Individuals with, and Parents of Individuals with Friedreich Ataxia Regarding Pre-symptomatic Testing of Minors.“轮椅的两面”:弗里德赖希共济失调患者及其父母对未成年人症状前检测的看法
J Genet Couns. 2015 Oct;24(5):732-43. doi: 10.1007/s10897-014-9801-9. Epub 2015 Jan 17.
6
The undiscovered country: the future of integrating genomic information into the EHR.未知领域:将基因组信息整合到电子健康记录中的未来
Genet Med. 2013 Oct;15(10):842-5. doi: 10.1038/gim.2013.130. Epub 2013 Sep 26.
7
Guidelines for disclosing genetic information to family members: from development to use.
Fam Cancer. 2006;5(1):103-16. doi: 10.1007/s10689-005-2581-5.
8
Establishment of a method of anonymization of DNA samples in genetic research.建立基因研究中DNA样本匿名化的方法。
J Hum Genet. 2003;48(6):327-330. doi: 10.1007/s10038-003-0022-6. Epub 2003 May 15.