Genetic counseling.
出版信息
Am J Hum Genet. 1975 Mar;27(2):240-2.
Abstract
摘要
相似文献
1
Genetic counseling.遗传咨询
Am J Hum Genet. 1975 Mar;27(2):240-2.
2
Genetics and genetic counseling in orthopedics.骨科中的遗传学与遗传咨询。
ONA J. 1975 Aug;2(8):194-201.
3
Impact of genetics on society.
Birth Defects Orig Artic Ser. 1987;23(2):1-5.
4
[Responsibilities in the use of human genetics].[人类遗传学应用中的责任]
Orv Hetil. 1973 Oct 7;114(40):2401-4.
5
Recommendations of the European society of human genetics on genetic testing for common disorders.欧洲人类遗传学会关于常见疾病基因检测的建议。
Genet Test Mol Biomarkers. 2011 May;15(5):291-2. doi: 10.1089/gtmb.2011.1519.
6
7
Genetics 1978: progress and problems.《遗传学1978：进展与问题》
Ariz Med. 1978 Jul;35(7):464-6.
8
General review of medical genetics.医学遗传学概论
Adv Otorhinolaryngol. 2000;56:1-10. doi: 10.1159/000059079.
9
The human face of genetics.遗传学的人文面孔。
Nurs Times. 1990;86(41):43-5.
10
Guide to genetics services information.遗传学服务信息指南。
Lamp. 1995 May;52(4):40.
引用本文的文献
1
Genetic self-counselors in Tunisia: the role of health education in hemoglobinopathies prevention among high school students.突尼斯的基因自我咨询者：健康教育在高中生血红蛋白病预防中的作用。
Orphanet J Rare Dis. 2025 Aug 13;20(1):426. doi: 10.1186/s13023-025-03958-z.
2
Genetic counseling development and milestone in Oman.阿曼的遗传咨询发展与里程碑
Genet Med Open. 2024 Oct 18;2(Suppl 2):101897. doi: 10.1016/j.gimo.2024.101897. eCollection 2024.
3
Genetic counseling: development of requirements, contents, and quality management in Germany.遗传咨询：德国相关要求、内容及质量管理的发展
Med Genet. 2021 May 14;33(1):45-52. doi: 10.1515/medgen-2021-2056. eCollection 2021 Apr.
4
Genetic Counselling Improves the Molecular Characterisation of Dementing Disorders.遗传咨询改善痴呆症的分子特征分析。
J Pers Med. 2021 May 26;11(6):474. doi: 10.3390/jpm11060474.
5
Evaluation of the results of patients who applied to the Çukurova University, Medical Genetics Department for prenatal diagnosis and determination of genetic counseling principles.评估向库尤罗瓦大学医学遗传学系申请产前诊断和确定遗传咨询原则的患者的结果。
Turk J Med Sci. 2021 Apr 30;51(2):657-660. doi: 10.3906/sag-2004-298.
6
Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide.罕见病的新生儿筛查和携带者筛查：创新如何在全球范围内挑战筛查标准。
J Community Genet. 2021 Apr;12(2):257-265. doi: 10.1007/s12687-020-00488-y. Epub 2020 Oct 19.
7
Meeting Patients' Right to the Correct Diagnosis: Ongoing International Initiatives on Undiagnosed Rare Diseases and Ethical and Social Issues.满足患者获得正确诊断的权利：罕见病未确诊问题的国际持续行动和伦理社会问题。
Int J Environ Res Public Health. 2018 Sep 21;15(10):2072. doi: 10.3390/ijerph15102072.
8
Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practices.学术医疗中心普通及专科遗传咨询师临床工作量评估：一种评估遗传咨询实践的工具。
NPJ Genom Med. 2016 May 11;1:16010. doi: 10.1038/npjgenmed.2016.10. eCollection 2016.
9
Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.自找麻烦：普通人群中的预防性基因组测序与患者选择的作用
Am J Bioeth. 2015;15(7):3-14. doi: 10.1080/15265161.2015.1039721.
10
Systemically-Based Psychotherapeutic Techniques in Genetic Counseling.遗传咨询中基于系统的心理治疗技术
J Genet Couns. 1997 Mar;6(1):1-20. doi: 10.1023/A:1025630917735.
Zotero 插件