Evaluating Anti-SmD1-amino-acid 83-119 Peptide Reactivity in Children with Systemic Lupus Erythematosus and Other Immunological Diseases

por Yang, Hai-Ou, Zhang, Xiao-Qing, Fu, Qi-Hua
Publicado 2016

Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion

por Xu, Yue-Juan, Chen, Sun, Zhang, Jian, Fang, Shao-Hai, Guo, Qian-Qian, Wang, Jian, Fu, Qi-Hua, Li, Fen, Xu, Rang, Sun, Kun
Publicado 2014

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

por Xu, Yue-Juan, Wang, Jian, Xu, Rang, Zhao, Peng-Jun, Wang, Xi-Ke, Sun, Heng-Juan, Bao, Li-Ming, Shen, Jie, Fu, Qi-Hua, Li, Fen, Sun, Kun
Publicado 2011

De novo disruptive heterozygous MMP21 variants are potential predisposing genetic risk factors in Chinese Han heterotaxy children

por Qin, Xi-ji, Xu, Meng-meng, Ye, Jia-jun, Niu, Yi-wei, Wu, Yu-rong, Xu, Rang, Li, Fen, Fu, Qi-hua, Chen, Sun, Sun, Kun, Xu, Yue-juan
Publicado 2022

Cardiac Computed Tomography-Derived Left Atrial Strain and Volume in Pediatric Patients With Congenital Heart Disease: A Comparative Analysis With Transthoracic Echocardiography

por Xie, Wei-Hui, Chen, Li-Jun, Hu, Li-Wei, Ouyang, Rong-Zhen, Guo, Chen, Sun, Ai-Min, Wang, Qian, Qiu, Hai-Sheng, Zhang, Yu-Qi, Zhang, Hao, Fu, Qi-Hua, Zhong, Yu-Min
Publicado 2022