Prenatal CNV detection by means of exome sequencing instead of microarray diagnostics: one test fits all!D. Westra,R. Pfundt,S. J. C. Stevens,I. Feenstra,C. F. H. A. Gilissen,K. Neveling,M. R. Nelen,H. G. Yntema,D. F. C. M. Smeets,N. de Leeuw,B. H. W. FaasEUROPEAN JOURNAL OF HUMAN GENETICS（2019）引用 0|浏览55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
