Bo Wang
4PUBLICATIONS
4CO-AUTHORS
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Publications (4)
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|Jul 17, 2023
Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies.Yibo Lu, Yiyang Zhou, Jing Guo
|Feb 22, 2023
Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease.Yibo Lu, Qing Fang, Ming Qi
|Jun 08, 2021
<i>SORBS2</i> is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients.Fei Liang, Bo Wang, Juan Geng
|May 08, 2020
15q11.2 deletion is enriched in patients with total anomalous pulmonary venous connection.Xiaoliang Li, Guocheng Shi, Yang Li
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