Whole genome sequencing yields medically significant secondary variants in similar to 25% of a paediatric cohortM. Meyn,S. C. Bowdin,C. Marshall,D. J. Stavropoulos, R. Basran,M. Reuter,D. Merico,R. Z. Hayeems,M. Szego,R. Zlotnik Shaul,C. Shuman, T. Nalpathamkalam, G. Pellecchia,B. Thiruvahindrapuram,M. Girdea,M. Brudno,R. D. Cohn,S. W. Scherer,P. N. Ray,N. MonfaredEUROPEAN JOURNAL OF HUMAN GENETICS(2018)引用 0|浏览45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