Shuangzhu Lin
6PUBLICATIONS
9CO-AUTHORS
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Publications (6)
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|Jan 10, 2026
Cartilage-hair hypoplasia in a patient with compound heterozygous variants in the RMRP gene: A case report.Shuangzhu Lin, Qiandui Chen, Yangfan Qi
|Nov 20, 2025
Idiopathic isolated adrenocorticotropic hormone deficiency combined with testicular germ cell tumor: Case report.Ming Yang, Shuangzhu Lin, Dongting Fu
|Sep 09, 2025
Phelan-McDermid syndrome in a Chinese pediatric patient: A case report - new heterozygous mutations lead to PMS.Shuangzhu Lin, XiaoYu Sun, Ying Zhou
|Jun 16, 2023
A case of Sandhoff disease caused by a novel β-hexosaminidase B (HEXB) mutation c.118delG (p.A40fs*24): A case report from China.Hongyan Xie, Shuangzhu Lin, Yang Chen
|Apr 28, 2023
Thyroid hormone resistance resulting from a novel mutation in the THRB gene in a Chinese child: A case report.Jinhua Feng, Shuangzhu Lin, Wei Wang
|Apr 07, 2023
A nonsense mutation in the CUL3 gene in a Chinese patient with autism spectrum disorder and epilepsy: A case report.Meijia Qian, Shuangzhu Lin, Yangyang Tan
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