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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.
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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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genomics%22">BMC Medical Genomics</searchLink>. 10/21/2022, Vol. 15, p1-10. 10p.
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        Value: 10.1186/s12920-022-01227-7
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              Text: 10/21/2022
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              Y: 2022
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