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Neuropsychiatric Disease and Treatment|April 22, 2015
An association study between DLGAP1 rs11081062 and EFNA5 rs26728 polymorphisms with obsessive-compulsive disorder in a Chinese Han populationJiang Li, Jiajia Cui, Xiuhai Wang, et al.Clinical Endocrinology|April 17, 2014
Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genesFang Wang, Kunna Lu, Zhifeng Yang, et al.American Journal of Nephrology|May 26, 2012
High-frequency variant p.T60M in NaCl cotransporter and blood pressure variability in Han ChineseLeping Shao, Yanhua Lang, Yan Wang, et al.Pregnancy Hypertension|December 12, 2018
The relationship between DNA repair genes (XPA, XPF, XPG) polymorphism and the risk of preeclampsia in Chinese Han WomenHaiyan Wang, Jingjing Liu, Ru Zhang, et al.Clinical, Cosmetic and Investigational Dermatology|July 2, 2024
A Novel Ectodysplasin a Gene mutation of X-Linked Hypohidrotic Ectodermal DysplasiaYuan Zhuang, Ru Zhang, Miaomiao Li, et al.Rheumatology International|August 15, 2014
The CC chemokine ligand 2 (CCL2) polymorphism -2518A/G is associated with gout in the Chinese Han male populationRuixia Sun, Keke Zhang, Xiaokun Zhang, et al.Pregnancy Hypertension|September 30, 2025
Association of SIRT1 rs12415800 and SIRT6 rs350844 polymorphisms with preeclampsia: A case-control studyChao Zhu, Longqiang Xu, Fumin Zheng, et al.Journal of Labelled Compounds & Radiopharmaceuticals|March 28, 2025
Synthesis, Preclinical Characterizations and Imaging Studies of [18F]AlF-Labeled NY104, a CAIX-Targeting Diagnostic AgentYu Huang, Waisi Eng, Chong Shao, et al.The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|January 17, 2017
Choline acetyltransferase may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control studyXiuling Yang, Wenmiao Liu, Mingji Yi, et al.International Journal of Cardiology|October 27, 2009
CFC1 mutations in Chinese children with congenital heart diseaseBinbin Wang, Jing Wang, Shiguo Liu, et al.Pageof 22