Wei Zhang
4PUBLICATIONS
3CO-AUTHORS

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Publications (4)
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|Feb 25, 2026
Congenital Hypogonadotropic Hypogonadism Caused by Prokineticin Receptor 2 Rare Sequence Variants: Molecular Genetics, Clinical Phenotypes and Therapeutic Outcomes From a Single-center Cohort.Yuhan Wang, Wei Zhang, Jiangfeng Mao
|Jan 27, 2025
MYRF Variants in Patients With 46,XY Differences/Disorders of Sex Development and Literature Review.Wei Zhang, Xi Wang, Jiangfeng Mao
|May 06, 2023
The genetic spectrum of a Chinese series of patients with 46, XY disorders of the sex development.Wei Zhang, Jiangfeng Mao, Xi Wang
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