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Rui Guo

2PUBLICATIONS

2CO-AUTHORS

Developmental genetics (incl. sex determination)Gene mapping

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Publications (2)

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|Feb 10, 2024

Bi-allelic variants in chromatoid body protein TDRD6 cause spermiogenesis defects and severe oligoasthenoteratozoospermia in humans.

Rui Guo, Huan Wu, Xiaoyu Zhu

|Sep 22, 2022

Biallelic loss-of-function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans.

Guanxiong Wang, Xiaoyu Zhu, Yang Gao

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Xiaojin He

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Hao Geng

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Xiaojin He

1 joint publications

Hao Geng

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