Search Results - "Meng, Guiquan"

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  1. 1

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

    Published in Frontiers in genetics (05-08-2022)
    “…Infertility is a global health concern. has been found to be associated with premature ovarian insufficiency (POI) and non-obstructive azoospermia (NOA), but…”
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    Journal Article
  2. 2

    Identification of a missense variant of MND1 in meiotic arrest and non-obstructive azoospermia by Zhao, Jingpeng, Ji, Zhiyong, Meng, Guiquan, Luo, Jiaqiang, Zhang, Yuxiang, Ou, Ningjing, Bai, Haowei, Tian, Ruhui, Zhi, Erlei, Huang, Yuhua, Liu, Nachuan, He, Wenbin, Tan, Yueqiu, Li, Zheng, Yao, Chencheng, Li, Peng

    Published in Journal of human genetics (01-11-2023)
    “…Meiotic arrest is a common pathologic phenotype of non-obstructive azoospermia (NOA), yet its genetic causes require further investigation. Meiotic nuclear…”
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    Journal Article
  3. 3

    Reclassification of DMD Duplications as Benign: Recommendations for Cautious Interpretation of Variants Identified in Prenatal Screening by He, Wenbin, Meng, Guiquan, Hu, Xiao, Dai, Jing, Liu, Jiyang, Li, Xiurong, Hu, Hao, Tan, Yueqiu, Zhang, Qianjun, Lu, Guangxiu, Lin, Ge, Du, Juan

    Published in Genes (28-10-2022)
    “…Duplications are the main type of dystrophin gene (DMD) variants, which typically cause dystrophinopathies such as Duchenne muscular dystrophy and Becker…”
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    Journal Article
  4. 4

    Reclassification of IDMD/I Duplications as Benign: Recommendations for Cautious Interpretation of Variants Identified in Prenatal Screening by He, Wenbin, Meng, Guiquan, Hu, Xiao, Dai, Jing, Liu, Jiyang, Li, Xiurong, Hu, Hao, Tan, Yueqiu, Zhang, Qianjun, Lu, Guangxiu, Lin, Ge, Du, Juan

    Published in Genes (01-10-2022)
    “…Duplications are the main type of dystrophin gene (DMD) variants, which typically cause dystrophinopathies such as Duchenne muscular dystrophy and Becker…”
    Get full text
    Journal Article