Non-invasive prenatal testing (NIPT) for 22q11.2 deletion syndrome using a targeted microarray-based cell-free (cfDNA) testM. Schmid,E. Wang,P. Bogard, J. Zahn,C. Hacker,R. Stokowski,S. Wang,K. White,A. SparksEUROPEAN JOURNAL OF HUMAN GENETICS（2018）引用 0|浏览38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
