Clinical and Genetic Study of children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation.

JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION（2019）

引用 12|浏览17

暂无评分

摘要

Supplemental Digital Content is available in the text

查看译文

关键词

children,de novo mutation,hereditary cancer,Peutz-Jeghers syndrome,polyposis syndrome,STK11

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