Corrigendum to “Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene” [Stem Cell Res. 56 (2021) 102517] von Zu, Bailing, Zhang, Xiaoqing, You, Guoling, Fu, Qihua

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SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients von Liang, Fei, Wang, Bo, Geng, Juan, You, Guoling, Fa, Jingjing, Zhang, Min, Sun, Hunying, Chen, Huiwen, Fu, Qihua, Zhang, Xiaoqing, Zhang, Zhen

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Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot von You, Guoling, Zu, Bailing, Wang, Bo, Fu, Qihua, Li, Fen

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Molecular Characteristics of Community-Associated Staphylococcus aureus Isolates From Pediatric Patients With Bloodstream Infections Between 2012 and 2017 in Shanghai, China von Wang, Xing, Liu, Qian, Zhang, He, Li, Xia, Huang, Weichun, Fu, Qihua, Li, Min

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Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene von Zu, Bailing, Zhang, Xiaoqing, You, Guoling, Fu, Qihua

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Identification of a novel ANO5 missense mutation in a Chinese family with familial florid osseous dysplasia von Lv, Mingming, You, Guoling, Wang, Jinbing, Fu, Qihua, Gupta, Anand, Li, Jun, Sun, Jian

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Hemodynamic Effects of A Simplified Venturi Conduit for Fontan Circulation: A Pilot, In Silico Analysis von Zhu, Fang, Shi, Guocheng, Wen, Chen, Zhang, Qian, Fu, Qihua, Liu, Jinlong, Zhu, Zhongqun, Chen, Huiwen

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Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation von Jiang, Xuechao, Li, Tingting, Liu, Sijie, Fu, Qihua, Li, Fen, Chen, Sun, Sun, Kun, Xu, Rang, Xu, Yuejuan

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Molecular Characteristic and Virulence Gene Profiles of Community-Associated Methicillin-Resistant Staphylococcus aureus Isolates from Pediatric Patients in Shanghai, China von Wang, Xing, Li, Xia, Liu, Wei, Huang, Weichun, Fu, Qihua, Li, Min

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MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation von Zhang, Erge, Yang, Jianping, Liu, Yang, Hong, Nanchao, Xie, Huilin, Fu, Qihua, Li, Fen, Chen, Sun, Yu, Yu, Sun, Kun

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The clinical application and laboratory management of molecular genetic diagnosis in children's hospital von Bao, Wenjie, Fu, Qihua, Zhang, Xiaoqing, Mo, Xi, Yu, Tingting

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Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4 von Li, Baolei, Li, Zhuoyan, Yang, Jianping, Hong, Nanchao, Jin, Lihui, Xu, Yuejuan, Fu, Qihua, Sun, Kun, Yu, Yu, Lu, Yanan, Chen, Sun

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A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease von Zhang, Xiaoqing, Wang, Jian, Wang, Bo, Chen, Sun, Fu, Qihua, Sun, Kun

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Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle von Zhang, Xingyu, Wang, Bo, You, Guoling, Xiang, Ying, Fu, Qihua, Yu, Yongguo, Zhang, Xiaoqing

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Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting von Zhang, Xiaoqing, Wang, Bo, Zhang, Lichen, You, Guoling, Palais, Robert A, Zhou, Luming, Fu, Qihua

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A Novel Nonsense GLI3 Variant Is Associated With Polydactyly and Syndactyly in a Family by Blocking the Sonic Hedgehog Signaling Pathway von Xiang, Ying, Li, Xiaoliang, Zhan, Zhiyan, Feng, Jue, Cai, Haiqing, Li, Yanxin, Fu, Qihua, Xu, Yunlan, Jiang, Hong, Zhang, Xiaoqing

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FGD5-AS1 Is a Hub lncRNA ceRNA in Hearts With Tetralogy of Fallot Which Regulates Congenital Heart Disease Genes Transcriptionally and Epigenetically von Zhang, Xingyu, Gao, Yunqian, Zhang, Xiaoping, Zhang, Xiaoqing, Xiang, Ying, Fu, Qihua, Wang, Bo, Xu, Zhuoming

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Multifunctional superparamagnetic nanoshells: combining two-photon luminescence imaging, surface-enhanced Raman scattering and magnetic separation von Jin, Xiulong, Li, Haiyan, Wang, Shanshan, Kong, Ni, Xu, Hong, Fu, Qihua, Gu, Hongchen, Ye, Jian

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Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing von Xie, Huilin, Zhang, Erge, Hong, Nanchao, Fu, Qihua, Li, Fen, Chen, Sun, Yu, Yu, Sun, Kun

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Exome sequencing reveals a novel nonsense mutation of GLI3 in a Chinese family with 'non-syndromic' pre-axial polydactyly von Xiang, Ying, Wang, Zhigang, Bian, Jingxia, Xu, Yunlan, Fu, Qihua

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