Haibin Guo
2PUBLICATIONS
4CO-AUTHORS
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Publications (2)
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|Nov 19, 2025
Novel DNAH17 Splice-Site Mutations Truncating the AAA6 Domain Cause Asthenozoospermia with MMAF.Leilei Feng, Feng Wan, Chenchen Cui
|Jan 29, 2024
Compound heterozygous mutations in CFTR causing congenital bilateral absence of the vas deferens in a Chinese pedigree.Lingyi Li, Xiaowei Qu, Chenchen Cui
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