Search Results - Bingbing Wu

Diagnostic biomolecules and combination therapy for pre-eclampsia by Jingqi Qi, Bingbing Wu, Xiuying Chen, Wei Wei, Xudong Yao

Connect to this object online.

A novel TSC2 missense variant associated with a variable phenotype of tuberous sclerosis complex: case report of a Chinese family by Feng Wang, Shiyi Xiong, Lin Wu, Maya Chopra, Xihong Hu, Bingbing Wu

Connect to this object online.

Novel PAK3 gene missense variant associated with two Chinese siblings with intellectual disability: a case report by Yanyan Qian, Bingbing Wu, Yulan Lu, Wenhao Zhou, Sujuan Wang, Huijun Wang

Connect to this object online.

Antimicrobial resistance prediction by clinical metagenomics in pediatric severe pneumonia patients by Mingyu Gan, Yanyan Zhang, Gangfeng Yan, Yixue Wang, Guoping Lu, Bingbing Wu, Weiming Chen, Wenhao Zhou

Connect to this object online.

Thirteen New Patients of <i>PPP2R5D</i> Gene Mutation and the Fine Profile of Genotype-Phenotype Correlation Unraveling the Pathogenic Mechanism Underlying Macrocephaly Phenotype by Yinmo Jiang, Bingbing Wu, Xi Zhang, Lin Yang, Sujuan Wang, Huiping Li, Shuizhen Zhou, Yanyan Qian, Huijun Wang

Connect to this object online.

Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants by Xiang Chen, Kai Yan, Yanyan Gao, Huijun Wang, Guoqiang Chen, Bingbing Wu, Qian Qin, Lin Yang, Wenhao Zhou

Connect to this object online.

Case Report: Progressive Cholestasis: Severe Phenotype of MEGDEL Syndrome With SATB2-Associated Syndrome by Yajie Su, Yajie Su, Hui Zhang, Huijun Wang, Bingbing Wu, Jiao Yang, Wenhao Zhou, Wenhao Zhou, Wenhao Zhou, Long Li

Connect to this object online.

Case report: A novel truncating variant of BCL11B associated with rare feature of craniosynostosis and global developmental delay by Xuemei Zhao, Bingbing Wu, Huiyao Chen, Ping Zhang, Yanyan Qian, Xiaomin Peng, Xinran Dong, Yaqiong Wang, Gang Li, Chenbin Dong, Huijun Wang

Connect to this object online.

Novel aggrecan variant, p. Gln2364Pro, causes severe familial nonsyndromic adult short stature and poor growth hormone response in Chinese children by Dandan Xu, Chengjun Sun, Zeyi Zhou, Bingbing Wu, Lin Yang, Zhuo Chang, Miaoying Zhang, Li Xi, Ruoqian Cheng, Jinwen Ni, Feihong Luo

Connect to this object online.

A Chinese girl of Blau syndrome with renal arteritis and a literature review by Qiaoqian Zeng, Haimei Liu, Guomin Li, Yifan Li, Wanzhen Guan, Tao Zhang, Yinv Gong, Xiaomei Zhang, Qianying Lv, Bingbing Wu, Hong Xu, Li Sun

Connect to this object online.

Galloway-Mowat Syndrome Type 3 Caused by OSGEP Gene Variants: A Case Report and Literature Review by Suhua Xu, Lan Hu, Lin Yang, Lin Yang, Bingbing Wu, Yun Cao, Yun Cao, Rong Zhang, Xin Xu, Haiyan Ma, Wenhao Zhou, Wenhao Zhou, Wenhao Zhou, Wenhao Zhou, Guoqiang Cheng, Peng Zhang, Liyuan Hu

Connect to this object online.

Further delineation of EBF3-related syndromic neurodevelopmental disorder in twelve Chinese patients by Jitao Zhu, Wenhui Li, Sha Yu, Wei Lu, Qiong Xu, Sujuan Wang, Yanyan Qian, Qiufang Guo, Suzhen Xu, Yao Wang, Ping Zhang, Xuemei Zhao, Qi Ni, Renchao Liu, Xu Li, Bingbing Wu, Shuizhen Zhou, Huijun Wang

Connect to this object online.

Neonatal Metabolic Acidosis in the Neonatal Intensive Care Unit: What Are the Genetic Causes? by Haiyan Ma, Zezhong Tang, Feifan Xiao, Long Li, Yangfang Li, Wenyan Tang, Liping Chen, Wenqing Kang, Yulan Lu, Xinran Dong, Guoqiang Cheng, Laishuan Wang, Wei Lu, Lin Yang, Qi Ni, Xiaomin Peng, Yao Wang, Yun Cao, Bingbing Wu, Wenhao Zhou, Wenhao Zhou, Deyi Zhuang, Guang Lin, Huijun Wang

Connect to this object online.

Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort by Xue Yang, Yaqi Li, Ye Fang, Hua Shi, Tianchao Xiang, Jiaojiao Liu, Jialu Liu, Xiaoshan Tang, Xiaoyan Fang, Jing Chen, Yihui Zhai, Qian Shen, Yunli Bi, Yanyan Qian, Bingbing Wu, Huijun Wang, Wenhao Zhou, Duan Ma, Haitao Bai, Jianhua Mao, Lizhi Chen, Xiaowen Wang, Xiaojie Gao, Ruifeng Zhang, Jieqiu Zhuang, Aihua Zhang, Xiaoyun Jiang, Hong Xu, Jia Rao

Connect to this object online.