A novel variant in SLC16A2 associated with typical Allan-Herndon-Dudley syndrome: a case report by Xiaodan Chen, Li Liu, Chunhua Zeng

Connect to this object online.

Thyroid function in children with Prader-Willi syndrome in Southern China: a single-center retrospective case series by Xinjiang Huang, Xi Yin, Dongyan Wu, Yanna Cai, Xiuzhen Li, Wen Zhang, Chunhua Zeng, Xiaojian Mao, Li Liu

Connect to this object online.

Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China by Aijing Xu, Jing Cheng, Huiying Sheng, Zhe Wen, Yunting Lin, Zhihong Zhou, Chunhua Zeng, Yongxian Shao, Cuiling Li, Li Liu, Xiuzhen Li

Connect to this object online.

Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature review by Xiaojian Mao, Sichi Liu, Yunting Lin, Zhen Chen, Yongxian Shao, Qiaoli Yu, Haiying Liu, Zhikun Lu, Huiyin Sheng, Xinshuo Lu, Yonglan Huang, Li Liu, Chunhua Zeng

Connect to this object online.

Clinical characteristics and long-term outcomes of 12 children with vitamin D-dependent rickets type 1A: A retrospective study by Yunting Lin, Zhihong Guan, Huifen Mei, Wen Zhang, Zhizi Zhou, Ling Su, Jing Cheng, Ruidan Zheng, Cuili Liang, Yanna Cai, Xi Yin, Dongyan Wu, Li Liu, Chunhua Zeng

Connect to this object online.