Myopia, developmental delay and a new mutation in ASXL1: a case report of Bohring-Opitz syndromeF. Guidolin,A. M. Spinelli,F. Faletra, M. Faleschini,I. Bruno,P. Magini,A. Fabretto,P. GaspariniEUROPEAN JOURNAL OF HUMAN GENETICS（2019）引用 0|浏览19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
