《人类突变》是一本同行评审的期刊,提供关于人类突变研究广泛方面的原始研究文章、方法、突变更新、评论、数据库文章、快速通信和信件的出版。欢迎有关新的DNA变异及其表型结果的报告、对基因组分析有价值的SNPs报告、对新的分子检测方法的描述以及临床诊断的新方法。在基因组水平上的基因组织的新报告,在突变研究的背景下,可以考虑。该杂志提供了一个独特的论坛,交流思想,方法和应用的兴趣分子,人类,医学遗传学家在学术,工业和临床研究设置世界各地。
Human Mutation is a peer-reviewed journal that offers publication of original Research Articles, Methods, Mutation Updates, Reviews, Database Articles, Rapid Communications, and Letters on broad aspects of mutation research in humans. Reports of novel DNA variations and their phenotypic consequences, reports of SNPs demonstrated as valuable for genomic analysis, descriptions of new molecular detection methods, and novel approaches to clinical diagnosis are welcomed. Novel reports of gene organization at the genomic level, reported in the context of mutation investigation, may be considered. The journal provides a unique forum for the exchange of ideas, methods, and applications of interest to molecular, human, and medical geneticists in academic, industrial, and clinical research settings worldwide.
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