CEP128 is involved in spermatogenesis in humans and mice von Zhang, Xueguang, Wang, Lingbo, Ma, Yongyi, Wang, Yan, Liu, Hongqian, Liu, Mohan, Qin, Lang, Li, Jinghong, Jiang, Chuan, Zhang, Xiaojian, Shan, Xudong, Liu, Yuliang, Li, Jinsong, Li, Yaqian, Zheng, Rui, Sun, Yongkang, Sun, Jianfeng, Leng, Xiangyou, Liang, Yan, Zhang, Feng, Jiang, Xiaohui, Yang, Yihong, Shen, Ying

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Application of thin slice technology of loose cuttings sample in early stage of experimental geology von Xiangpeng, Kong, Bihan, Qiu, Yanjie, Li, Jingsheng, Li, Yan, Shen, Yuming, Wu, Lihong, Jin, Yongyi, Ma, Pengpeng, Sheng, Yang, Liu

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X Chromosome Inactivation Pattern and Pregnancy Outcome of Female Carriers of Pathogenic Heterozygous X-Linked Deletions von Zhao, Yuanyin, Li, Jia, Dai, Limeng, Ma, Yongyi, Bai, Yun, Guo, Hong

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Prenatal diagnosis identifies compound heterozygous variants in RYR1 that causes ultrasound abnormalities in a fetus von Zhao, Qiuling, Li, Xiaoduo, Liu, Li, Zhang, Xu, Pan, Xin, Yao, Hong, Ma, Yongyi, Tan, Bo

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Prenatal Diagnosis and Genetic Analysis of 21q21.1-q21.2 Aberrations in Seven Chinese Pedigrees von Hu, Huamei, Zhang, Rong, Ma, Yongyi, Luo, Yanmei, Pan, Yan, Xu, Juchun, Jiang, Lupin, Wang, Dan

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Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1 von Lin, Tingting, Ma, Yongyi, Zhou, Danni, Sun, Liwei, Chen, Ke, Xiang, Yezhou, Tong, Keya, Jia, Chaoli, Jiang, Kean, Liu, Dongyun, Huang, Guoning

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Study of seismic attributes recognition method of high quality igneous rock reservoir von Yitong, Wang, Jingsheng, Li, Zandong Sun, Sam, Wei, Qiao, Yanjie, Li, Yongyi, Ma, Yan, Shen, Shuheng, Wang

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Novel biallelic variants in COL7A1 cause recessive dystrophic epidermolysis bullosa von Yang, Neng, Ma, Yongyi, Yao, Hong, Chang, Qing, Zhang, Victor, Liang, Zhiqing, Cai, Xiongwei

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Analysis of logging parameter model of Jurassic complex reservoir in Xinjiang Shenquan Oilfield von Li, Yanjie, Wang, Yitong, Ding, Hansheng, Ma, Yongyi, Shen, Yan, Chu, Lilan, Nie, Zhiyang, Du, Jinxia, Shao, Zhaoyi, Gao, Qicai, Wang, Shuheng

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An assessment of the analytical performance of non‐invasive prenatal testing (NIPT) in detecting sex chromosome aneuploidies: 34,717‐patient sample in a single prenatal diagnosis C... von Luo, Yanmei, Hu, Huamei, Zhang, Rong, Ma, Yongyi, Pan, Yan, Long, Yang, Hu, Bin, Yao, Hong, Liang, Zhiqing

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BRD4L cooperates with MYC to block local tumor invasion via suppression of S100A10 von Ma, Yongyi, Liu, Nan, Shi, Yu, Ma, Shuyan, Wang, Yingjun, Zheng, Wen, Sun, Rong, Song, Yihua, Chen, Miaomiao, Qu, Lishuai, Mao, Renfang, Fan, Yihui

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Copy number variation of functional RBMY1 is associated with sperm motility: an azoospermia factor-linked candidate for asthenozoospermia von Yan, Yuanlong, Yang, Xiling, Liu, Yunqiang, Shen, Ying, Tu, Wenling, Dong, Qiang, Yang, Dong, Ma, Yongyi, Yang, Yuan

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A retrospective analysis the clinic data and follow-up of non-invasive prenatal test in detection of fetal chromosomal aneuploidy in more than 40,000 cases in a single prenatal dia... von Luo, Yanmei, Hu, Huamei, Jiang, Luping, Ma, Yongyi, Zhang, Rong, Xu, Juchun, Pan, Yan, Long, Yang, Yao, Hong, Liang, Zhiqing

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Primary azoospermia factor C duplication associated with spermatogenic impariment: a case–control study based on Y‐chromosome haplogrouping in a Han Chinese population von Xie, Shengyu, Ma, Yongyi, Liu, Yunqiang, Tao, Dachang, Wang, Zhaokun, Yang, Yuan

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Preimplantation Genetic Screening with Spent Culture Medium/Blastocoel Fluid for in Vitro Fertilization von Li, Penghao, Song, Zhe, Yao, Yaxin, Huang, Tianhua, Mao, Rurong, Huang, Jun, Ma, Yongyi, Dong, Xin, Huang, Wenlong, Huang, Jihua, Chen, Tianjian, Qu, Ting, Li, Lingxiao, Zhong, Ying, Gu, Jiang

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Evidence for the involvement of the proximal copy of the MAGEA9 gene in Xq28-linked CNV67 specific to spermatogenic failure von Shen, Ying, Xu, Jinyan, Yang, Xiling, Liu, Yunqiang, Ma, Yongyi, Yang, Dong, Dong, Qiang, Yang, Yuan

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Fetal Phenotype and Prenatal Diagnosis of Kabuki Syndrome von Pan, Yan, Yao, Hong, Chen, Gongli, Tan, Qiong, Chang, Qing, Ma, Yongyi, Liang, Zhiqing

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Loss-of-function mutations in CEP78 cause male infertility in humans and mice von Zhang, Xueguang, Zheng, Rui, Liang, Chen, Liu, Haotian, Zhang, Xiaozhen, Ma, Yongyi, Liu, Mohan, Zhang, Wei, Yang, Yang, Liu, Man, Jiang, Chuan, Ren, Qingjia, Wang, Yan, Chen, Suren, Yang, Yihong, Shen, Ying

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Combined analysis of genome-wide-linked susceptibility loci to Kawasaki disease in Han Chinese von Yan, Yuanlong, Ma, Yongyi, Liu, Yunqiang, Hu, Hongde, Shen, Ying, Zhang, Sizhong, Ma, Yongxing, Tao, Dachang, Wu, Qing, Peng, Qian, Yang, Yuan

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Prenatal diagnosis of familial submicroscopic duplication at 18q22.3 without phenotypic abnormalities von Hu, Huamei, Ma, Yongyi, Zhang, Rong, Xu, Juchun, Hu, Bin, Long, Yang, Xu, Liang, Yao, Hong, Liang, Zhiqing

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