Genotype and phenotype correlation in a cohort of Chinese congenital hypothyroidism patients with DUOX2 mutations

por Zheng, Zhangqian, Yang, Lin, Sun, Chengjun, Wu, Jing, Luo, Feihong, Zhou, Wenhao, Lu, Wei
Publicado 2020

Genotype and phenotype analysis of a cohort of patients with congenital hyperinsulinism based on DOPA-PET CT scanning

por Ni, Jinwen, Ge, Jingjie, Zhang, Miaoying, Hussain, Khalid, Guan, Yihui, Cheng, Ruoqian, Xi, Li, Zheng, Zhangqian, Ren, Shuhua, Luo, Feihong
Publicado 2019

Phenotypes and epigenetic errors in patients with Beckwith-Wiedemann syndrome in China

por Zhang, Miaoying, Sun, Chengjun, Liu, Renchao, Dong, Chenbin, Cheng, Ruoqian, Zheng, Zhangqian, Wu, Bingbing, Luo, Feihong, Pei, Zhou, Lu, Wei
Publicado 2020

Genetic aetiology of primary adrenal insufficiency in Chinese children

por Chang, Zhuo, Lu, Wei, Zhao, Zhuhui, Xi, Li, Li, Xiaojing, Ye, Rong, Ni, Jinwen, Pei, Zhou, Zhang, Miaoying, Cheng, Ruoqian, Zheng, Zhangqian, Sun, Chengjun, Wu, Jing, Luo, Feihong
Publicado 2021