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Author/Creator Su, Lilan

1. Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice. (29th April 2022)

Authors:
Wang, Weili; Meng, Lanlan; He, Jiaxin; Su, Lilan; Li, Yong; Tan, Chen; Xu, Xilin; Nie, Hongchuan; Zhang, Huan; Du, Juan; Lu, Guangxiu; Luo, Mengcheng; Lin, Ge; Tu, Chaofeng; Tan, Yue-Qiu
Journal:
Molecular human reproduction
Issue:
Volume 28:Number 6(2022)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Issue 4 (3rd January 2023)

Authors:
He, Jiaxin; Liu, Qiang; Wang, Weili; Su, Lilan; Meng, Lanlan; Tan, Chen; Zhang, Huan; Zhang, Qianjun; Lu, Guangxiu; Du, Juan; Lin, Ge; Tu, Chaofeng; Tan, Yue‐Qiu
Journal:
Clinical genetics
Issue:
Volume 103:Issue 4(2023)
Page Start:
495
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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