Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mengjie Wang"'
Autor:
Juyi Li, Yuanyuan Li, Haichun Ni, Zhibin Yang, Jian Chen, Yarong Li, Sheng Ding, Xiaowan Jiang, Mengjie Wang, Li Li, Xiaoyu Lv, Xiaoyun Ruan, Qian Jiang, Zhang Lei, Yong Cheng, Juan Huang, Aiping Deng
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Lynch syndrome (LS) is an inherited autosomal dominant disorder caused by germline mutations of mismatch repair (MMR) genes, including MSH2, MSH6, PMS2, and MLH1. This study aimed to analyze the molecular defects and clinical manifestations of an aff
Externí odkaz:
https://doaj.org/article/f1065cd2ed5c42f3b9c17f5a90ce85aa
Autor:
Qian Jiang, Juan Huang, Xiaoyu Lv, Jian Chen, Juyi Li, Yong Cheng, Zhibin Yang, Mengjie Wang, Haichun Ni, Xiaoyun Ruan, Xiaowan Jiang, Aiping Deng, Yarong Li, Li Li, Yuanyuan Li, Sheng Ding, Zhang Lei
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Lynch syndrome (LS) is an inherited autosomal dominant disorder caused by germline mutations of mismatch repair (MMR) genes, including MSH2, MSH6, PMS2, and MLH1. This study aimed to analyze the molecular defects and clinical manifestations of an aff
Autor:
Juyi, Li, Yuanyuan, Li, Haichun, Ni, Zhibin, Yang, Jian, Chen, Yarong, Li, Sheng, Ding, Xiaowan, Jiang, Mengjie, Wang, Li, Li, Xiaoyu, Lv, Xiaoyun, Ruan, Qian, Jiang, Zhang, Lei, Yong, Cheng, Juan, Huang, Aiping, Deng
Publikováno v:
Frontiers in Oncology
Lynch syndrome (LS) is an inherited autosomal dominant disorder caused by germline mutations of mismatch repair (MMR) genes, including MSH2, MSH6, PMS2, and MLH1. This study aimed to analyze the molecular defects and clinical manifestations of an aff