Risultati della ricerca - Li, Huanzheng

Mitochondrial DNA Variants and Common Diseases: A Mathematical Model for the Diversity of Age-Related mtDNA Mutations di 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) di 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) di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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 di 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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