C7orf2 gene is interrupted within intronic region by a de novo reciprocal chromosomal translocation t (5,7)(q11, q36) in a patient with preaxial polydactyly.
AMERICAN JOURNAL OF HUMAN GENETICS(2001)
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
AMERICAN JOURNAL OF HUMAN GENETICS(2001)