Combinatorial approach of in silico and in vitro evaluation of MLH1 variant associated with Lynch syndrome like metastatic colorectal cancer

por Saleem, Komal, Zaib, Tahir, Ji, Wei, Zhang, Chunhui, Qin, Qian, Wang, Yusi, Xu, Lidan, Yu, Hanfei, Zhu, Siqi, Dong, Kexian, Si, Shuhan, Jia, Xueyuan, Wu, Jie, Fu, Songbin, Sun, Wenjing
Publicado 2020

A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family

por Zaib, Tahir, Ji, Wei, Saleem, Komal, Nie, Guangchen, Li, Chao, Cao, Lin, Xu, Baijun, Dong, Kexian, Yu, Hanfei, Hao, Xuguang, Xue, Yan, Si, Shuhan, Jia, Xueyuan, Wu, Jie, Zhang, Xuelong, Guan, Rongwei, Ji, Guohua, Bai, Jing, Chen, Feng, Liu, Yong, Sun, Wenjing, Fu, Songbin
Publicado 2019