Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new? by Wei-Li Wang, Chao-Feng Tu, Yue-Qiu Tan

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Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia by Yurong Wang, Ling Liu, Chen Tan, Guiquan Meng, Lanlan Meng, Lanlan Meng, Lanlan Meng, Lanlan Meng, Hongchuan Nie, Juan Du, Juan Du, Juan Du, Guang-Xiu Lu, Guang-Xiu Lu, Guang-Xiu Lu, Guang-Xiu Lu, Ge Lin, Ge Lin, Ge Lin, Ge Lin, Wen-Bin He, Wen-Bin He, Wen-Bin He, Wen-Bin He, Wen-Bin He, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan

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Risk Factors Affecting Alternate Segregation in Blastocysts From Preimplantation Genetic Testing Cycles of Autosomal Reciprocal Translocations by Pingyuan Xie, Pingyuan Xie, Pingyuan Xie, Liang Hu, Liang Hu, Liang Hu, Liang Hu, Yangqin Peng, Yue-qiu Tan, Yue-qiu Tan, Yue-qiu Tan, Yue-qiu Tan, Keli Luo, Keli Luo, Keli Luo, Keli Luo, Fei Gong, Fei Gong, Fei Gong, Fei Gong, Guangxiu Lu, Guangxiu Lu, Guangxiu Lu, Guangxiu Lu, Ge Lin, Ge Lin, Ge Lin, Ge Lin

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In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency by Wen-Juan Xiao, Wen-Bin He, Wen-Bin He, Wen-Bin He, Ya-Xin Zhang, Lan-Lan Meng, Lan-Lan Meng, Guang-Xiu Lu, Guang-Xiu Lu, Guang-Xiu Lu, Ge Lin, Ge Lin, Ge Lin, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan, Juan Du, Juan Du, Juan Du

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A novel loss-of-function variant in PNLDC1 inducing oligo-astheno-teratozoospermia and male infertility by Si-Yi Zhao, Lan-Lan Meng, Zhao-Li Du, Yue-Qiu Tan, Wen-Bin He, Xiong Wang

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Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings by Aixiang Luo, Dehua Cheng, Shimin Yuan, Haiyu Li, Juan Du, Yang Zhang, Chuanchun Yang, Ge Lin, Wenyong Zhang, Yue-Qiu Tan

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A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome by Shi-Min Yuan, Huan Huang, Chao-Feng Tu, Juan Du, Da-Bao Xu, Ge Lin, Guang-Xiu Lu, Yue-Qiu Tan

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DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice by Shushu Zhou, Shimin Yuan, Jintao Zhang, Lanlan Meng, Xin Zhang, Siyu Liu, Guangxiu Lu, Ge Lin, Mingxi Liu, Yue-Qiu Tan

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Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella by Lanlan Meng, Lanlan Meng, Qiang Liu, Qiang Liu, Chen Tan, Xilin Xu, Xilin Xu, Wenbin He, Wenbin He, Tongyao Hu, Chaofeng Tu, Chaofeng Tu, Yong Li, Juan Du, Juan Du, Qianjun Zhang, Qianjun Zhang, Qianjun Zhang, Guangxiu Lu, Guangxiu Lu, Guangxiu Lu, Li-Qing Fan, Li-Qing Fan, Li-Qing Fan, Ge Lin, Ge Lin, Ge Lin, Hongchuan Nie, Huan Zhang, Huan Zhang, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan

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Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency by Ya‐Xin Zhang, Wen‐Bin He, Wen‐Juan Xiao, Lan‐Lan Meng, Chen Tan, Juan Du, Guang‐Xiu Lu, Ge Lin, Yue‐Qiu Tan

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A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans by Yong Li, Wei-Li Wang, Chao-Feng Tu, Lan-Lan Meng, Tong-Yao Hu, Juan Du, Ge Lin, Hong-Chuan Nie, Yue-Qiu Tan

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Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency by Wen-Bin He, Yue-Qiu Tan, Xiao Hu, Wen Li, Bo Xiong, Ke-Li Luo, Fei Gong, Guang-Xiu Lu, Ge Lin, Juan Du

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A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance by Rui‐Qi Bai, Wen‐Bin He, Qian Peng, Su‐Hui Shen, Qian‐Qian Yu, Juan Du, Yue‐Qiu Tan, Yue‐Hong Wang, Bin‐Jie Liu

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Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans by Dong-Yan Li, Xiao-Xuan Yang, Chao-Feng Tu, Wei-Li Wang, Lan-Lan Meng, Guang-Xiu Lu, Yue-Qiu Tan, Qian-Jun Zhang, Juan Du

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Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis by Jian-Wen Hou, Xiao-Liang Li, Li Wang, Cong-Ling Dai, Na Li, Xiao-Hui Jiang, Yue-Qiu Tan, Er-Po Tian, Qin-Tong Li, Wen-Ming Xu

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Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature by Haiyu Li, Juan Du, Wen Li, Dehua Cheng, Wenbin He, Duo Yi, Bo Xiong, Shimin Yuan, Chaofeng Tu, Lanlan Meng, Aixiang Luo, Ge Lin, Guangxiu Lu, Yue-Qiu Tan

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Improving native human sperm freezing protection by using a modified vitrification method by Dai Zhou, Xing-Ming Wang, Rui-Xue Li, Yi-Ze Wang, Yuan-Chi Chao, Zhi-Zhong Liu, Zeng-Hui Huang, Hong-Chuan Nie, Wen-Bing Zhu, Yue-Qiu Tan, Li-Qing Fan

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Non-invasive preimplantation genetic testing for conventional IVF blastocysts by Pingyuan Xie, Shuoping Zhang, Yifang Gu, Bo Jiang, Liang Hu, Yue-qiu Tan, Yaxin Yao, Yi Tang, Anqi Wan, Sufen Cai, Yangyun Zou, Guangxiu Lu, Cheng Wan, Fei Gong, Sijia Lu, Ge Lin

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Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression by Chaofeng Tu, Junfei Wen, Weili Wang, Qifan Zhu, Ying Chen, Jianglu Cheng, Zeye Li, Lanlan Meng, Yong Li, Wenbin He, Chen Tan, Chunbo Xie, Shao-Mei Fu, Juan Du, Guangxiu Lu, Ge Lin, Lan-Tao Gou, Yue-Qiu Tan

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Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192 by Jihong Guo, Wen-Bin He, Lei Dai, Fen Tian, Zhenqing Luo, Fang Shen, Ming Tu, Yu Zheng, Liu Zhao, Chen Tan, Yongteng Guo, Lan-Lan Meng, Wei Liu, Mei Deng, Xinghan Wu, Yu Peng, Shuju Zhang, Guang-Xiu Lu, Ge Lin, Hua Wang, Yue-Qiu Tan, Yongjia Yang

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