Clinical and whole exome sequencing findings in children from Yunnan Yi minority ethnic group with retinitis pigmentosa: two case reports

por Xiao, Yi-shuang, He, Wen-Ji, Jiang, Hong-chao, Tan, Li, Ma, Jing, Zhang, Zhen
Publicado 2023

DLEU1 promotes cell survival by preventing DYNLL1 degradation in esophageal squamous cell carcinoma

por Li, Qihang, Zhang, Zhiyu, Jiang, HongChao, Hou, Jun, Chai, Yuhang, Nan, Hongxing, Li, Feng, Wang, Lianghai
Publicado 2022

Elastic fiber degradation in the development of pediatric granuloma annulare: Report of 39 cases

por Zhang, Dong-Yuan, Zhang, Li, Yang, Qin-Yan, Xie, Yu-Cheng, Jiang, Hong-Chao, Li, Jia-Zheng, Shu, Hong
Publicado 2023

Diagnostic value of bone marrow cell morphology in visceral leishmaniasis-associated hemophagocytic syndrome: Two case reports

por Shi, Shu-Lan, Zhao, Heng, Zhou, Beng-Jiang, Ma, Ming-Biao, Li, Xiao-Juan, Xu, Ji, Jiang, Hong-Chao
Publicado 2022

A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I

por Ma, Jing, Lin, Ken, Jiang, Hong‐chao, Yang, Yanli, Zhang, Yu, Yang, Guilian, Sun, Hao, Ming, Cheng, Bi, Xianyun, Zhang, Tiesong, Ruan, Biao
Publicado 2019

Next generation sequencing of RB1gene for the molecular diagnosis of ethnic minority with retinoblastoma in Yunnan

por Zhang, Zhen, Xiao, Yi-shuang, Shen, Ru, Jiang, Hong-chao, Tan, Li, Li, Ren-qiu, Yang, Xiao-hong, Gu, Huai-yu, He, Wen-Ji, Ma, Jing
Publicado 2020