Atypical deletion of Williams–Beuren syndrome reveals the mechanism of neurodevelopmental disorders.
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| Title: | Atypical deletion of Williams–Beuren syndrome reveals the mechanism of neurodevelopmental disorders. |
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| Authors: | Zhou, Jianrong1,2 (AUTHOR), Zheng, Ying3 (AUTHOR), Liang, Guiying4 (AUTHOR), Xu, Xiaoli5 (AUTHOR), Liu, Jian1 (AUTHOR), Chen, Shaoxian2,6 (AUTHOR), Ge, Tongkai1 (AUTHOR), Wen, Pengju1,6 (AUTHOR), Zhang, Yong1 (AUTHOR), Liu, Xiaoqing7 (AUTHOR), Zhuang, Jian1,2 (AUTHOR), Wu, Yueheng1,2,4 (AUTHOR) edgar_wu@aliyun.com, Chen, Jimei1,2 (AUTHOR) jimei_1965@outlook.com |
| Source: | BMC Medical Genomics. 10/21/2022, Vol. 15, p1-10. 10p. |
| Database: | Academic Search Ultimate |
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