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Seizure|May 10, 2026
Genetic characterization of DDX11 variants identified in a Chinese family with Warsaw breakage syndromeXue Zhong, Wenmiao Liu, Xueping Zheng, et al.
Plos One|February 19, 2016
Genetic Analysis of IL-17 Gene Polymorphisms in Gout in a Male Chinese Han PopulationZheng Zhou, Xinde Li, Hua Li, et al.
Optics Letters|June 5, 2012
Fast photorefractive response of vanadium-doped lithium niobate in the visible regionYinfeng Dong, Shiguo Liu, Yongfa Kong, et al.
International Journal of Psychiatry in Medicine|April 30, 2015
rs2043211 polymorphism in CARD8 is not associated with Tourette syndrome in a family-based association study in the Chinese Han populationMingji Yi, Xiaohui Shao, Jianhua Ma, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 10, 2014
[Association of serotonin transporter linked polymorphic region 44 bp variable number of tandem repeat polymorphism with Tourette syndrome]Ying Zhang, Nailun Su, Guiju Wang, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 20, 2015
Role of Toll-Like Receptor 3 Gene Polymorphisms in PreeclampsiaAiping Chen, Congying Li, Jingli Wang, et al.
Plos One|June 10, 2021
Correction: Study of reference intervals for free triiodothyronine, free thyroxine, and thyroid-stimulating hormone in an elderly Chinese Han populationJingting Xiong, Shiguo Liu, Kai Hu, et al.
Plos One|September 24, 2020
Study of reference intervals for free triiodothyronine, free thyroxine, and thyroid-stimulating hormone in an elderly Chinese Han populationJingting Xiong, Shiguo Liu, Kai Hu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 17, 2022
Whole-exome sequencing analysis to identify novel potential pathogenetic NPC1 mutations in two Chinese families with Niemann-Pick disease type CChengcheng Guan, Xinhui Gan, Chengqing Yang, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|August 18, 2021
The first Chinese case of Vici syndrome with novel compound heterozygous sequence variants in EPG5Liping Dong, Liangshan Li, Xiao Zhang, et al.
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