Sprouty loss of function mutations in the mouse results in defects characteristic of 22q11 deletion syndrome, which are exacerbated by Tbx1 haploinsufficiency
DEVELOPMENTAL BIOLOGY(2011)
AI 理解论文
溯源树
样例
![](https://originalfileserver.aminer.cn/sys/aminer/pubs/mrt_preview.jpeg)
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要
DEVELOPMENTAL BIOLOGY(2011)