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Evaluation of current genetic testing reports in German-speaking countries with regard to secondary use and future electronic implementation

Modern diagnostic methods (next-generation sequencing) are one of the current hopes with regard to a personalised medicine. By applying detailed genetic analysis, it is possible to not only improve the prediction of potential risks (as, e.g., concerning hereditary breast cancer) but also the precisi...

詳細記述

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書誌詳細
出版年:Eur J Hum Genet
主要な著者: Radke, Teja Falk, Patton, Simon J., Pantazoglou, Elisabeth, Sass, Julian, Thun, Sylvia
フォーマット: Artigo
言語:Inglês
出版事項: Springer International Publishing 2020
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7170954/
https://ncbi.nlm.nih.gov/pubmed/32055015
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-020-0586-z
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