DDX3X mutations in 11 french patients with intellectual disability : new phenotypic features V. Ruault,C. Coubes,P. Charles,M. Vincent,M. Nizon,C. Mignot,A. Delahaye-Duriez,C. Thauvin,N. Jean-Marcais,A. Garde,L. Faivre,Y. Alembik, A. Gouronc,B. Durand,C. Nava,B. Keren,C. Depienne,F. Tran Mau Them,M. Willems,B. Gerard,D. GenevieveEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 0|浏览28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