Yunting Lin
11PUBLICATIONS
24CO-AUTHORS
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Publications (11)
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|Nov 12, 2025
Clinical characteristics, genetic spectrum and therapeutic effects of 51 male patients with idiopathic hypogonadotropic hypogonadism from southern China.Huiying Sheng, Cuili Liang, Jing Cheng
|May 22, 2024
Biochemical and molecular analysis of pediatric patients with metachromatic leukodystrophy in South China: functional characterization of five novel ARSA variants.Taolin Li, Yonglan Huang, Chunyan Tao
|Oct 23, 2023
The third case of Marbach-Rustad progeroid syndrome caused by a de novo LEMD2 variant.Zhikun Lu, Wen Zhang, Xiaojian Mao
|Jun 06, 2023
Co-occurrence of Spondyloepiphyseal Dysplasia and X-Linked Hypophosphatemia in a Three-Generation Chinese Family.Jian Ma, Ye Zhang, Xiaoxiao Ding
|Jun 27, 2022
The first Chinese case of Siddiqi syndrome caused by a homozygous FITM2 variant.Yunting Lin, Wen Zhang, Duan Li
|Sep 06, 2021
Two De Novo Mosaic Variants Within the Same Site of PHEX Gene in a Girl with X-Linked Hypophosphatemic Rickets.Yunting Lin, Wen Zhang, Xinjiang Huang
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