De novo ARX mutations in female patients with agenesis of the corpus callosum and intellectual disability M. Taveira,S. Heide,C. Mignot,M. Milh,A. Rastetter,A. Jacquette,P. Charles,I. Marey,S. Whalen,B. Keren,C. Nava,D. HeronEUROPEAN JOURNAL OF HUMAN GENETICS（2018）引用 0|浏览18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
