Case report: A novel truncating variant of <i>BCL11B</i> associated with rare feature of craniosynostosis and global developmental delay.

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第一作者： Xuemei,Zhao

第一单位： Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai, China.

作者： Xuemei,Zhao ^[1] ; Bingbing,Wu ^[1] ; Huiyao,Chen ^[1] ; Ping,Zhang ^[1] ; Yanyan,Qian ^[1] ; Xiaomin,Peng ^[1] ; Xinran,Dong ^[1] ; Yaqiong,Wang ^[1] ; Gang,Li ^[1] ; Chenbin,Dong ^[2] ; Huijun,Wang ^[1]

作者单位： Center for Molecular Medicine, Children's Hospital of Fudan University, Shanghai, China. ^[1] Department of Plastic Surgery, Children's Hospital of Fudan University, Shanghai, China. ^[2]

关键词 BCL11B craniosynostosis developmental delay pediatrics truncating variation

DOI 10.3389/fped.2022.982361

PMID 36275064

发布时间 2022-10-25

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Frontiers in pediatrics

2022年10卷

982361页

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Case report: A novel truncating variant of <i>BCL11B</i> associated with rare feature of craniosynostosis and global developmental delay.

Frontiers in pediatrics

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Frontiers in pediatrics

相关期刊

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Case report: A novel truncating variant of <i>BCL11B</i> associated with rare feature of craniosynostosis and global developmental delay.

Frontiers in pediatrics

相似文献

Frontiers in pediatrics

相关期刊

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