检索结果 - Li, Huanzheng

Mitochondrial DNA Variants and Common Diseases: A Mathematical Model for the Diversity of Age-Related mtDNA Mutations 由 Li, Huanzheng, Slone, Jesse, Fei, Lin, Huang, Taosheng

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Delineation variable genotype/phenotype correlations of 6q27 terminal deletion derived from dic(6;18)(q27;p10) 由 Zhou, Lili, Chen, Chong, Li, Huanzheng, Chen, Yunying, Xu, Xueqin, Lin, Xiaoling, Tang, Shaohua

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Erratum to: Delineation variable genotype/phenotype correlations of 6q27 terminal deletion derived from dic(6;18)(q27;p10) 由 Zhou, Lili, Chen, Chong, Li, Huanzheng, Chen, Yunying, Xu, Xueqin, Lin, Xiaoling, Tang, Shaohua

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Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations 由 Xu, Chenyang, Xiang, Yanbao, Xu, Xueqin, Zhou, Lili, Li, Huanzheng, Dong, Xueqin, Tang, Shaohua

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Mutation analysis and prenatal diagnosis of a family with congenital contractural arachnodactyly 由 Hu, Lin, Li, Huanzheng, Sun, Guang, Wu, Ke, Luan, Zhaotang, Xiang, Yanbao, Tang, Shaohua

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Subtelomeric multiplex ligation-dependent probe amplification as a supplement for rapid prenatal detection of fetal chromosomal aberrations 由 Chen, Xiangnan, Li, Huanzheng, Mao, Yijian, Xu, Xueqin, Lv, Jiaojiao, Zhou, Lili, Lin, Xiaoling, Tang, Shaohua

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Erratum to: Subtelomeric multiplex ligation-dependent probe amplification as a supplement for rapid prenatal detection of fetal chromosomal aberrations 由 Chen, Xiangnan, Li, Huanzheng, Mao, Yijian, Xu, Xueqin, Lv, Jiaojiao, Zhou, Lili, Lin, Xiaoling, Tang, Shaohua

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Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism 由 Xu, Chenyang, Xiang, Yanbao, Li, Huanzheng, Xu, Yunzhi, Mao, Yijian, Zhou, Lili, Xu, Xueqin, Tang, Shaohua

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The variations in human orphan G protein‐coupled receptor QRFPR affect PI3K‐AKT‐mTOR signaling 由 Li, Huanzheng, Lou, Ran, Xu, Xueqin, Xu, Chenyang, Yu, Yuan, Xu, Yunzhi, Hu, Lin, Xiang, Yanbao, Lin, Xuan, Tang, Shaohua

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The distal arthrogryposis‐linked p.R63C variant promotes the stability and nuclear accumulation of TNNT3 由 Lu, Jinfang, Li, Huanzheng, Zhang, He, Lin, Zhengxiu, Xu, Chenyang, Xu, Xueqin, Hu, Lin, Luan, Zhaotang, Lou, Yongliang, Tang, Shaohua

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Skeleton Genetics: a comprehensive database for genes and mutations related to genetic skeletal disorders 由 Chen, Chong, Jiang, Yi, Xu, Chenyang, Liu, Xinting, Hu, Lin, Xiang, Yanbao, Chen, Qingshuang, Chen, Denghui, Li, Huanzheng, Xu, Xueqin, Tang, Shaohua

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Clinical application of single‐molecule optical mapping to a multigeneration FSHD1 pedigree 由 Zhang, Qian, Xu, Xueqin, Ding, Lirong, Li, Huanzheng, Xu, Chengyang, Gong, Yuyan, Liu, Ying, Mu, Ting, Leigh, Don, Cram, David S., Tang, Shaohua

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Enhanced inflammation and suppressed adaptive immunity in COVID-19 with prolonged RNA shedding 由 Tang, Xiaohua, Sun, Rui, Ge, Weigang, Mao, Tingting, Qian, Liujia, Huang, Chongquan, Kang, Zhouyang, Xiao, Qi, Luo, Meng, Zhang, Qiushi, Li, Sainan, Chen, Hao, Liu, Wei, Wang, Bingjie, Li, Shufei, Lin, Xiaoling, Xu, Xueqin, Li, Huanzheng, Wu, Lianpeng, Dai, Jianyi, Gao, Huanhuan, Li, Lu, Lu, Tian, Liang, Xiao, Cai, Xue, Ruan, Guan, Xu, Fei, Li, Yan, Zhu, Yi, Kong, Ziqing, Huang, Jianping, Guo, Tiannan

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