Results
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Novel THRB mutation analysis in congenital hypothyroidism with thyroid dysgenesis. [electronic resource] by
- Zhou, Zhixia
- Yang, Chengyu
- Lv, Fuyan
- Liu, Wenmiao
- Yan, Shengli
- Zang, Hongwei
- Li, Miaomiao
- Wang, Fang
- Zang, Yucui
- Liu, Shiguo
Producer: 20191010
In:
Journal of cellular biochemistry vol. 119
Availability: No items available.
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3.
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Genetic testing of PAX8 mutations associated with thyroid dysgenesis in Chinese congenital hypothyroidism patients. [electronic resource] by
- Li, Miaomiao
- Wang, Fang
- Wang, Xiuli
- Zang, Yucui
- Liu, Wenmiao
- Wang, Fengqi
- Zhang, Lu
- Tang, Qian
- Liu, Shiguo
- Zhao, Dehua
Producer: 20210301
In:
Endokrynologia Polska vol. 71
Availability: No items available.
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4.
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Identification of Two Missense Mutations in [electronic resource] by
- Liu, Shiguo
- Han, Wenxiu
- Zang, Yucui
- Zang, Hongwei
- Wang, Fang
- Jiang, Pei
- Wei, Hongwei
- Liu, Xiangju
- Wang, Yangang
- Ma, Xu
- Ge, Yinlin
Publication details: Frontiers in endocrinology 2019
In:
Frontiers in endocrinology vol. 10
Availability: No items available.
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5.
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Mutations in ASH1L confer susceptibility to Tourette syndrome. [electronic resource] by
- Liu, Shiguo
- Tian, Miaomiao
- He, Fan
- Li, Jiani
- Xie, Hong
- Liu, Wenmiao
- Zhang, Yeting
- Zhang, Ru
- Yi, Mingji
- Che, Fengyuan
- Ma, Xu
- Zheng, Yi
- Deng, Hao
- Wang, Guiju
- Chen, Lang
- Sun, Xue
- Xu, Yinglei
- Wang, Jingli
- Zang, Yucui
- Han, Mengmeng
- Wang, Xiuhai
- Guan, Hongzai
- Ge, Yinlin
- Wu, Chunmei
- Wang, Haiyan
- Liang, Hui
- Li, Hui
- Ran, Ni
- Yang, Zhaochuan
- Huang, Huanhuan
- Wei, Yanzhao
- Zheng, Xueping
- Sun, Xiangrong
- Feng, Xueying
- Zheng, Lanlan
- Zhu, Tao
- Luo, Wenhan
- Chen, Qinan
- Yan, Yuze
- Huang, Zuzhou
- Jing, Zhongcui
- Guo, Yixia
- Zhang, Xuzhan
- Schaaf, Christian P
- Xing, Jinchuan
- Wang, Chuanyue
- Yu, Fuli
- Guan, Ji-Song
Producer: 20201207
In:
Molecular psychiatry vol. 25
Availability: No items available.
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