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38.
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Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes. [electronic resource] by
- Lin, Shan
- Zeng, Jia-Bin
- Zhao, Gui-Xian
- Yang, Zhen-Zhen
- Huang, Hui-Ping
- Lin, Min-Ting
- Wu, Zhi-Ying
- Wang, Ning
- Chen, Wan-Jin
- Fang, Ling
Producer: 20200306
In:
Seizure vol. 71
Availability: No items available.
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39.
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A "Triple Trouble" Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy. [electronic resource] by
- Lin, Xiao-Dan
- He, Jun-Jie
- Lin, Feng
- Chen, Hai-Zhu
- Xu, Liu-Qing
- Hu, Wei
- Cai, Nai-Qing
- Lin, Min-Ting
- Wang, Ning
- Wang, Zhi-Qiang
- Xu, Guo-Rong
Producer: 20181211
In:
Chinese medical journal vol. 131
Availability: No items available.
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40.
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Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency. [electronic resource] by
- Chen, Hai-Zhu
- Jin, Ming
- Cai, Nai-Qing
- Lin, Xiao-Dan
- Liu, Xin-Yi
- Xu, Liu-Qing
- Lin, Min-Ting
- Lin, Feng
- Wang, Ning
- Wang, Zhi-Qiang
- Xu, Guo-Rong
Producer: 20200106
In:
Chinese medical journal vol. 132
Availability: No items available.
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