The European Certificate in Medical Genetics and Genomics (ECMGG).

IF 4.6 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Peter D Turnpenny, Laura Pölsler, Ute Moog, Edward S Tobias, Angela Peron, Susanne E Boonen, Bonnie Lynch, Jonathan Berg
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引用次数: 0

Abstract

The European Certificate in Medical Genetics and Genomics (ECMGG) is the official knowledge-based, end-of-specialist training examination designed and delivered by the Union Européenne des Médecins Spécialistes - Section of Medical Genetics (UEMS-SMG). The examination is a joint venture of the SMG, the European Society of Human Genetics (ESHG), and the European Board of Medical Genetics (EBMG). Sittings have taken place in 2019 and 2021-24, and it is gaining in reputation as a high-quality, high-standard assessment. In 2024 the ECMGG underwent satisfactory appraisal by the UEMS-Council of European Specialist Medical Assessment (CESMA). This paper describes the development of the ECMGG, its structure, outcomes, and its meaning for the standards and harmonisation of the specialty of Medical Genetics throughout Europe.

欧洲医学遗传学和基因组学证书(ECMGG)。
欧洲医学遗传学和基因组学证书(ECMGG)是由欧盟医学遗传学部门(UEMS-SMG)设计和提供的以知识为基础的官方专业培训考试。该检查是SMG、欧洲人类遗传学学会(ESHG)和欧洲医学遗传学委员会(EBMG)的合资企业。该项目已于2019年和2021-24年举行,作为一项高质量、高标准的评估,它正在赢得声誉。2024年,欧洲医学专家评估委员会(CESMA)对欧洲医学专家评估小组进行了满意的评估。本文描述了ECMGG的发展,它的结构,结果,以及它对整个欧洲医学遗传学专业的标准和协调的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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