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Published in Molecular genetics & genomic medicine (01.06.2021)
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Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment
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Published in Brain (London, England : 1878) (01.08.2023)
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CNV profiles of Chinese pediatric patients with developmental disorders
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Published in Genetics in medicine (01.04.2021)
Published in Genetics in medicine (01.04.2021)
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Journal Article
Human iPSC-derived neuron of 16p11.2 deletion reveals haplotype-specific expression of MAPK3 and its contribution to variable NDD phenotypes
Liu, Fang, Chen, Liang, Li, Zhengchang, Sen, Zhao, Shangguan, Shaofang, Yuan, Haiming, Yao, Ruen, Qin, Zailong, Zhang, Shujie, Zou, Liping, Gao, Zhijie, Chen, Qian, Wen, Suiwen, Peng, Jing, Yin, Fei, Chen, Fei, Qiu, Xiaoxia, Luo, Jingsi, Xie, Yingjun, Lu, Dian, Zhang, Yu, Xie, Hua, Wang, Hongying, Cui, Xiaodai, Wang, Jian, Huang, Hailiang, Liu, Ruize, Sun, Xiaofang, Chen, Chao, Wu, Nan, Liu, Chunyu, Shen, Yiping, Gusella, James F, Chen, Xiaoli
Published in bioRxiv (11.07.2022)
Published in bioRxiv (11.07.2022)
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