Associated Papers
A case report of Culler-Jones syndrome with deafness carrying a novel mutation in GLI2 gene.
Yuan X et al.
Bmc Pediatrics, 2025
Clinical characteristics and genetic expansion of 46,XY disorders of sex development children in a Chinese prospective study.
Tang Y et al.
Endocrine Connections, 2023
Clinical Profiles and Genetic Spectra of 814 Chinese Children With Short Stature.
Li X et al.
The Journal of Clinical Endocrinology and Metabolism, 2022
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