The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation von Luo, Shiqiang, Chen, Xingyuan, Zeng, Dingyuan, Tang, Ning, Yuan, Dejian, Zhong, Qingyan, Mao, Aiping, Xu, Ruofan, Yan, Tizhen

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Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease von Zhu, Zuobin, Yuan, Dejian, Luo, Denghui, Lu, Xitong, Huang, Shi

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Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1 von Zhang, Xinrong, Wu, Jiebin, Zhou, Jianteng, Liang, Jie, Han, Yu, Qi, Yunmeng, Zhu, Tao, Yuan, Dejian, Zhu, Zuobin, Zhai, Jingfang

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Correction to: The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation von Luo, Shiqiang, Chen, Xingyuan, Zeng, Dingyuan, Tang, Ning, Yuan, Dejian, Zhong, Qingyan, Mao, Aiping, Xu, Ruofan, Yan, Tizhen

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Tandem Mass Spectrometry Screening for Inborn Errors of Metabolism in Newborns and High-Risk Infants in Southern China: Disease Spectrum and Genetic Characteristics in a Chinese Po... von Tan, Jianqiang, Chen, Dayu, Chang, Rongni, Pan, Lizhen, Yang, Jinling, Yuan, Dejian, Huang, Lihua, Yan, Tizhen, Ning, Haiping, Wei, Jiangyan, Cai, Ren

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Detection of four rare thalassemia variants using Single-molecule realtime sequencing von Luo, Shiqiang, Chen, Xingyuan, Zeng, Dingyuan, Tang, Ning, Yuan, Dejian, Liu, Bailing, Chen, Lizhu, Zhong, Qingyan, Li, Jiaqi, Liu, Yinyin, Chen, Jianping, Wang, Xiaoyuan, Yan, Tizhen

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Identification and Functional Characterization of a Novel Nonsense Variant in ARR3 in a Southern Chinese Family With High Myopia von Yuan, Dejian, Yan, Tizhen, Luo, Shiqiang, Huang, Jun, Tan, Jianqiang, Zhang, Jianping, Zhang, Victor Wei, Lan, Yueyuan, Hu, Taobo, Guo, Jing, Huang, Mingwei, Zeng, Dingyuan

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Prenatal diagnosis of paternal uniparental disomy for chromosome 2 in two fetuses with intrauterine growth restriction von Tan, Xuemei, Liu, Bailing, Yan, Tizhen, Wei, Xiaobao, Qin, Yanfeng, Zeng, Dingyuan, Yuan, Dejian

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Scoring the collective effects of SNPs： association of minor alleles with complex traits in model organisms von Yuan, DeJian, Zhu, ZuoBin, Tan, XiaoHua, Liang, Jie, Zeng, Chen, Zhang, JieGen, Chen, Jun, Ma, Long, Dogan, Ayca, Brockmann, Gudrun, Goldmann, Oliver, Medina, Eva, Rice, Amanda D., Moyer, Richard W., Man, Xian, Yi, Ke, Li, YanKe, Lu, Qing, Huang, YiMin, Huang, Shi

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The genetic equidistance result： misreading by the molecular clock and neutral theory and reinterpretation nearly half of a century later von Hu, TaoBo, Long, MengPing, Yuan, DeJian, Zhu, ZhuBing, Huang, YiMin, Huang, Shi

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Genetic equidistance at nucleotide level von Yuan, Dejian, Huang, Shi

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A Novel Homozygous Synonymous Variant in CCDC134 as a Cause of Osteogenesis Imperfecta Type XXII von Ning, Haiping, Liang, Cuili, Mei, Huifen, Yuan, Dejian, Wei, Xiaobao, Huang, Xiao, Tan, Dongdong, Tan, Jianqiang

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The relationship between the minor allele content and Alzheimer's disease von Chen, Hongyao, Lei, Xiaoyun, Yuan, Dejian, Huang, Shi

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Collective effects of common SNPs and risk prediction in lung cancer von Lei, Xiaoyun, Yuan, Dejian, Zhu, Zuobin, Huang, Shi

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Profiling of circulating extracellular vesicle microRNAs reveals diagnostic potential and pathways in non-obstructive and obstructive azoospermia von Qi, Yujuan, Wu, Yalun, Pang, Kun, Cao, Yijuan, Li, Honglin, Qiao, Yu, Yuan, Dejian, Liu, Xiangen, Li, Zhenbei, Hu, Fangfang, Yang, Wen, Han, Conghui, Zhu, Zuobin

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Accumulation of minor alleles and risk prediction in schizophrenia von He, Pei, Lei, Xiaoyun, Yuan, Dejian, Zhu, Zuobin, Huang, Shi

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Application of Copy Number Variation Sequencing in Genetic Analysis of Miscarriages in Early and Middle Pregnancy von Luo, Shiqiang, Chen, Xingyuan, Yan, Tizhen, Ya, Jiaolian, Xu, Zehui, Cai, Pengfei, Yuan, Dejian, Tang, Ning

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Optimizing peripheral blood chromosome analysis: effects of refrigeration time and blood volume von Wei, Xiaoni, Tang, Ning, Zhang, Ling, Wang, Wendan, Li, Yaxing, Qin, Jiangfeng, Yuan, Dejian, Wang, Yujiang

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Tumor suppressor RIZ1 in obesity and the PI3K/AKT/mTOR pathway von Xie, Xiaolei, Man, Xian, Zhu, Zuobin, Yuan, Dejian, Huang, Shi

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Close genetic relationships between a spousal pair with autism-affected children and high minor allele content in cases in autism-associated SNPs von Zhu, Zuobin, Lu, Xitong, Yuan, Dejian, Huang, Shi

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