Novel mutations of the SRF gene in Chinese sporadic conotruncal heart defect patients by Xu Mengmeng, Xu Yuejuan, Chen Sun, Lu Yanan, Li Fen, Sun Kun

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Conotruncal Heart Defects by Herlina Dimiati, Silfia Yasmine Lubis

Subjects: “…Conotruncal heart defects…”
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Placental DNA Methylation Abnormalities in Prenatal Conotruncal Heart Defects by Jingjing Liu, Jingjing Liu, Yuduo Wu, Yuduo Wu, Hairui Sun, Hairui Sun, Xiaowei Liu, Xiaowei Liu, Xiaoyan Gu, Xiaoyan Gu, Ying Zhao, Ying Zhao, Ye Zhang, Ye Zhang, Jiancheng Han, Jiancheng Han, Yihua He, Yihua He

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Maternal exposure to ambient ozone and fetal conotruncal heart defects in China: A multicenter cohort study by Yanping Ruan, Yaqi Wang, Jianhui Guo, Tingting Man, Xiaoyan Hao, Xiaoxue Zhou, Chenyu Wang, Hanyu Deng, Jing Li, Zhiyong Zou, Yihua He

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

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What is the impact of a novel MED12 variant on syndromic conotruncal heart defects? Analysis of case report on two male sibs by Silvia Amodeo, Giuseppe Vitrano, Melania Guardino, Giuseppe Paci, Fulvio Corselli, Vincenzo Antona, Giuseppe Barrano, Monia Magliozzi, Antonio Novelli, Renato Venezia, Giovanni Corsello

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Endothelial Notch1 Is Required for Proper Development of the Semilunar Valves and Cardiac Outflow Tract by Sara N. Koenig, Kevin Bosse, Uddalak Majumdar, Elizabeth M. Bonachea, Freddy Radtke, Vidu Garg

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22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects by Carolina Putotto, Flaminia Pugnaloni, Marta Unolt, Stella Maiolo, Matteo Trezzi, Maria Cristina Digilio, Annapaola Cirillo, Giuseppe Limongelli, Bruno Marino, Giulio Calcagni, Paolo Versacci

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New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects by Alaaeldin G. Fayez, PhD, Nora N. Esmaiel, PhD, Engy A. Ashaat, MD, Miral M. Refeat, PhD, Randa S. Lotfy, PhD, Haiam Abdel Raouf, PhD, Mona O. El Ruby, MD

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A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplica... by Nanchao Hong, Erge Zhang, Qingjie Wang, Xiaoqing Zhang, Fen Li, Qihua Fu, Rang Xu, Yu Yu, Sun Chen, Yuejuan Xu, Kun Sun

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Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population by Xike Wang, Haitao Wei, Ying Tian, Yue Wu, Lei Luo

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