这是谁的基因？关于乳腺癌基因检测引发的家族冲突的病例讨论。 - Suppr

Suppr

超能文献

Whose gene is it? A case discussion about familial conflict over genetic testing for breast cancer.

作者信息

Green Ronald M, Thomas A Mathew

出版信息

J Genet Couns. 1997 Jun;6(2):245-54. doi: 10.1023/a:1025672421311.

DOI:10.1023/a:1025672421311

PMID:11656643

Abstract

摘要

相似文献

Whose gene is it? A case discussion about familial conflict over genetic testing for breast cancer.这是谁的基因？关于乳腺癌基因检测引发的家族冲突的病例讨论。

J Genet Couns. 1997 Jun;6(2):245-54. doi: 10.1023/a:1025672421311.

Ethics of prediction: genetic risk and the physician-patient relationship.预测伦理：遗传风险与医患关系

Genome Sci Technol. 1995;1(1):21-36. doi: 10.1089/gst.1995.1.21.

Iceland's genetic $ell-out.冰岛的基因抛售。（你提供的原文中“$ell-out”应该有误，推测可能是“sell-out”，正确译文为：冰岛的基因售卖。）

Genewatch. 1999 Feb;12(1):12-3.

Genetic testing and individual rights.基因检测与个人权利。

Suffolk Univ Law Rev. 1993 Winter;27(4):1477-97.

In defence of ignorance: genetic information and the right not to know.为无知辩护：基因信息与不知情权。

Eur J Health Law. 1999 Jun;6(2):119-32. doi: 10.1163/15718099920522730.

IRB. 1993 Jul-Aug;15(4):7-11.

Privacy and disclosure in medical genetics examined in an ethics of care.在关怀伦理视角下审视医学遗传学中的隐私与信息披露问题。

Bioethics. 1991 Jul;5(3):212-32. doi: 10.1111/j.1467-8519.1991.tb00161.x.

Structuring the review of human genetics protocols, Part II: diagnostic and screening studies.构建人类遗传学研究方案的审查，第二部分：诊断与筛查研究。

IRB. 1997 May-Aug;19(3-4):1-13.

Genes and society: puzzles, promises, and policy.

Ann Am Acad Pol Soc Sci. 1997 Jan;549:173-84. doi: 10.1177/0002716297549001013.

Roundtable: the politics of genetic testing.圆桌会议：基因检测的政治学

Issues Sci Technol. 1996 Fall;13(1):48-54.

引用本文的文献

Managing Couple Conflict During Prenatal Counseling Sessions: An Investigation of Genetic Counselor Experiences and Perceptions.产前咨询期间处理夫妻冲突：对遗传咨询师经验与看法的调查

J Genet Couns. 2018 Sep;27(5):1275-1290. doi: 10.1007/s10897-018-0252-6. Epub 2018 Mar 22.

Family perspectives in lynch syndrome becoming a family at risk, patterns of communication and influence on relations.林奇综合征中的家庭观点：成为有风险的家庭、沟通模式及对关系的影响

Hered Cancer Clin Pract. 2012 May 25;10(1):6. doi: 10.1186/1897-4287-10-6.

What facilitates or impedes family communication following genetic testing for cancer risk? A systematic review and meta-synthesis of primary qualitative research.癌症风险基因检测后，哪些因素促进或阻碍了家庭沟通？一项关于原发性定性研究的系统评价和元综合分析。

J Genet Couns. 2010 Aug;19(4):330-42. doi: 10.1007/s10897-010-9296-y. Epub 2010 Apr 9.

Personal characteristics of older primary care patients who provide a buccal swab for apolipoprotein E testing and banking of genetic material: the spectrum study.为载脂蛋白E检测及基因材料储存提供颊拭子的老年初级保健患者的个人特征：光谱研究

Community Genet. 2004;7(4):202-10. doi: 10.1159/000082263.

Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statement.先天性听力损失病因诊断的遗传学评估指南。先天性听力损失遗传学评估专家小组。美国医学遗传学与基因组学学会声明。

Genet Med. 2002 May-Jun;4(3):162-71. doi: 10.1097/00125817-200205000-00011.

本文引用的文献

Huntington disease: a case study describing the complexities and nuances of predictive testing of monozygotic twins.亨廷顿舞蹈症：一项描述同卵双胞胎预测性检测的复杂性和细微差别的案例研究。

J Genet Couns. 1995 Jun;4(2):125-37. doi: 10.1007/BF01408635.

Regulatory aspects of the distinction between research and medical practice.研究与医疗实践区分的监管方面。

IRB. 1984 May-Jun;6(3):7-8.

Genetics and the dead: implications for genetics research with samples from deceased persons.

Am J Med Genet. 1997 Mar 31;69(3):332-4.

Familial breast cancer: a controlled study of risk perception, psychological morbidity and health beliefs in women attending for genetic counselling.家族性乳腺癌：对参加遗传咨询的女性的风险认知、心理发病率和健康信念的对照研究。

Br J Cancer. 1996 Aug;74(3):482-7. doi: 10.1038/bjc.1996.387.

BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes.遗传性乳腺癌-卵巢癌家族中的BRCA1检测。一项关于患者决策及结果的前瞻性研究。

JAMA. 1996 Jun 26;275(24):1885-92.

Genetic privacy: from the laboratory to the legislature.

Genome Res. 1995 Oct;5(3):209-13. doi: 10.1101/gr.5.3.209.

Developing strategies for intervention and prevention in hereditary breast cancer.

J Natl Cancer Inst Monogr. 1995(17):99-102.

Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium.家族性乳腺癌和卵巢癌的基因连锁分析：来自214个家庭的结果。乳腺癌连锁协会。

Am J Hum Genet. 1993 Apr;52(4):678-701.

Discussion points to consider in research related to the human genome.在与人类基因组相关的研究中需要考虑的讨论要点。

Hum Gene Ther. 1993 Aug;4(4):477-95. doi: 10.1089/hum.1993.4.4-477.

What about the family?那家人呢？

Hastings Cent Rep. 1990 Mar-Apr;20(2):5-10.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验