Discovery and characterisation of 49 novel genetic disorders from analysing de novo mutations in 31,058 parent child trio exomesJ. Kaplanis,K. Samocha, Z. Zhang,R. Torene,K. Arvai,S. Lelieveld, E. de Boer,E. Kucuk,R. Pfundt, L. van de Wiel, P. Danecek,J. McRae,G. Gallone,R. Eberhardt, H. Brunner,C. Gilissen,K. Retterer,M. HurlesEUROPEAN JOURNAL OF HUMAN GENETICS（2019）引用 1|浏览28暂无评分AI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
