Widening the spectrum of congenital anomalies related to a partial 21q monosomy detected prenatally A. Sajeva,F. Lalatta,T. Rizzuti,S. Boito,N. Persico, R. Silipigni,S. Guerneri,E. Scola,C. M. Cinnante,F. Triulzi,L. Ronzoni,C. Cesaretti,F. NatacciEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 0|浏览37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