Complete mitochondrial DNA sequence analysis in two southern Chinese pedigrees with Leber hereditary optic neuropathy revealed secondary mutations along with the primary mutation

Por Shu, Lei, Zhang, Yong-Ming, Huang, Xiao-Xiao, Chen, Chun-Yue, Zhang, Xian-Ning
Publicado em 2012

Deletion analysis of SMN1 and NAIP genes in southern Chinese children with spinal muscular atrophy

Por Liang, Yu-hua, Chen, Xiao-ling, Yu, Zhong-sheng, Chen, Chun-yue, Bi, Sheng, Mao, Lian-gen, Zhou, Bo-lin, Zhang, Xian-ning
Publicado em 2009

RET Germline Mutations Identified by Exome Sequencing in a Chinese Multiple Endocrine Neoplasia Type 2A/Familial Medullary Thyroid Carcinoma Family

Por Qi, Xiao-Ping, Ma, Ju-Ming, Du, Zhen-Fang, Ying, Rong-Biao, Fei, Jun, Jin, Hang-Yang, Han, Jian-Shan, Wang, Jin-Quan, Chen, Xiao-Ling, Chen, Chun-Yue, Liu, Wen-Ting, Lu, Jia-Jun, Zhang, Jian-Guo, Zhang, Xian-Ning
Publicado em 2011