Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID).Yuxia Chen,Xiang Tang,Ling Liu,Qinrong Huang,Li Lin, Guoqing Liu,Nong XiaoGenes & diseases（2021）引用 0|浏览1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
