Additional file 3 of Atypical deletion of Williams–Beuren syndrome reveals the mechanism of neurodevelopmental disorders
- Resource Type
- Authors
- Zhou, Jianrong; Zheng, Ying; Liang, Guiying; Xu, Xiaoli; Liu, Jian; Chen, Shaoxian; Ge, Tongkai; Wen, Pengju; Zhang, Yong; Liu, Xiaoqing; Zhuang, Jian; Wu, Yueheng; Chen, Jimei
- Source
- Subject
- congenital, hereditary, and neonatal diseases and abnormalities
cardiovascular diseases
- Language
Additional file 3: Table S3. Facial features of nine WBS patients with atypical deletion.