Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: A case report

por Lin, Shuang-Zhu, Zhou, Xin-Yu, Wang, Wan-Qi, Jiang, Kai
Publicado 2021

Dynamically loading IFC models on a web browser based on spatial semantic partitioning

por Lu, Hong-Lei, Wu, Jia-Xing, Liu, Yu-Shen, Wang, Wan-Qi
Publicado 2019

Novel compound heterozygous variants in the TAF6 gene in a patient with Alazami-Yuan syndrome: A case report

por Lin, Shuang-Zhu, Feng, Jin-Hua, Sun, Li-Ping, Ma, Hong-Wei, Wang, Wan-Qi, Li, Jia-Yi
Publicado 2022

VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report

por Wu, Xiao-Hui, Lin, Shuang-Zhu, Zhou, Yan-Qiu, Wang, Wan-Qi, Li, Jia-Yi, Chen, Qian-Dui
Publicado 2022

Clinical manifestations and gene analysis of Hutchinson-Gilford progeria syndrome: A case report

por Zhang, Su-Li, Lin, Shuang-Zhu, Zhou, Yan-Qiu, Wang, Wan-Qi, Li, Jia-Yi, Wang, Cui, Pang, Qi-Ming
Publicado 2022

Two novel mutations in the VPS33B gene in a Chinese patient with arthrogryposis, renal dysfunction and cholestasis syndrome 1: A case report

por Yang, Hui, Lin, Shuang-Zhu, Guan, Shi-Hui, Wang, Wan-Qi, Li, Jia-Yi, Yang, Gui-Dan, Zhang, Su-Li
Publicado 2022

Retroperitoneal leiomyoma located in the broad ligament: A case report

por Zhang, Xue-Song, Lin, Shuang-Zhu, Liu, Yu-Jiao, Zhou, Lei, Chen, Qian-Dui, Wang, Wan-Qi, Li, Jia-Yi
Publicado 2022

Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report

por Lin, Shuang-Zhu, Ma, Qi-Ji, Pang, Qi-Ming, Chen, Qian-Dui, Wang, Wan-Qi, Li, Jia-Yi, Zhang, Su-Li
Publicado 2022

Development and validation of the thyroid cancer self-perceived discrimination scale to identify patients at high risk for psychological problems

por Liu, Zhi-jin, Feng, Lin-sen, Li, Feng, Yang, Li-rong, Wang, Wan-qi, He, Yuan, Meng, Zong-ting, Wang, Yu-feng
Publicado 2023

Novel frameshift mutation in the AHDC1 gene in a Chinese global developmental delay patient: A case report

por Lin, Shuang-Zhu, Xie, Hong-Yan, Qu, Yan-Lai, Gao, Wen, Wang, Wan-Qi, Li, Jia-Yi, Feng, Xiao-Chun, Jin, Chun-Quan
Publicado 2022

A case of West syndrome and global developmental delay in a child with a heterozygous mutation in the TBL1XR1 gene: A case report

por Wu, Xiao-Hui, Lin, Shuang-Zhu, Liu, Zhen-Xian, Qi, Yang-Fan, Wang, Wan-Qi, Li, Jia-Yi, Chen, Qian-Dui, Yang, Lu-Lu
Publicado 2023

Children with infectious pneumonia caused by Ralstonia insidiosa: A case report

por Lin, Shuang-Zhu, Qian, Mei-Jia, Wang, Yan-Wei, Chen, Qian-Dui, Wang, Wan-Qi, Li, Jia-Yi, Yang, Rui-Tong, Wang, Xin-Yao, Mu, Chun-Yu, Jiang, Kai
Publicado 2023