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BMC Medical Genomics|June 6, 2025
Novel compound heterozygous DOCK6 variants expand the mutational spectrum in prenatal diagnosis of Adams-Oliver syndrome 2Xue Zhong, Xuan Zheng, Yinglei Xv, et al.International Journal of General Medicine|March 12, 2024
JAG1 Variants Confer Genetic Susceptibility to Thyroid Dysgenesis and Thyroid Dyshormonogenesis in 813 Congenital Hypothyroidism in ChinaMiaomiao Li, Xiaoyu Wang, Fang Wang, et al.Case Reports in Medicine|December 22, 2025
Identification of Novel IL-10RA Variant in Infantile-Onset Inflammatory Bowel Disease: A Case Series With Preliminary Genotype-Phenotype Correlation From Two Chinese FamiliesChengcheng Guan, Yuanxuan Ma, Xiao Zhang, et al.Scientific Reports|September 25, 2015
Associations between interleukin and interleukin receptor gene polymorphisms and risk of goutShiguo Liu, Zheng Zhou, Can Wang, et al.European Child & Adolescent Psychiatry|October 20, 2011
No significant association between Catechol-O-methyl transferase (COMT) -287A/G gene polymorphism and Tourette's syndrome in family-based association study in Chinese Han populationShiguo Liu, Mingji Yi, Fengguang Qi, et al.Neuroscience Letters|August 24, 2017
Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han populationWenmiao Liu, Shiyan Qiu, Chuanping Gao, et al.Journal of Attention Disorders|February 7, 2014
The Subjective Quality of Life in Young People With Tourette Syndrome in ChinaShiguo Liu, Lanlan Zheng, Xueping Zheng, et al.Neurocase|January 16, 2014
Family-based association study between monoamine oxidase A (MAOA) gene promoter VNTR polymorphism and Tourette's syndrome in Chinese Han populationShiguo Liu, Xueqin Wang, Longqiang Xu, et al.Reproductive Biology and Endocrinology : RB&E|November 19, 2025
Cell-free RNAs in maternal peripheral blood as potential biomarkers of preeclampsia: a reviewYuping Shan, Renmei Cai, Mengmeng Han, et al.International Journal of Clinical and Experimental Pathology|June 23, 2015
Association of IL-1α rs17561 and IL-1 RN rs315952 polymorphisms with Tourette syndrome: a family-based studyFan He, Xiaohui Shao, Mingji Yi, et al.Pageof 22