A novel mutation in MYCN gene causes an unusual presentation of Feingold syndromeA. Peleg,L. Sagi-Dain, V. Adir,A. Kurolap,C. Gonzaga-Jauregui,J. Overton, A. Mori,A. Shuldiner,H. Baris, R. WolsteinEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 0|浏览16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