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Molecular Medicine Reports|March 19, 2013
Transforming growth factor-β1 gene mutations and phenotypes in pediatric patients with Camurati‑Engelmann diseaseChun Wang, Bao-Hong Zhang, Yu-Juan Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 13, 2003
[Association of polymorphisms of vitamin D receptor gene start codon and 3'-end region with bone mineral density in postmenopausal women]Zhen-lin Zhang, Jin-xiu Zhao, Xun-wu Meng, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 21, 2017
Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical InterventionShan-Shan Li, Jin-We He, Wen-Zhen Fu, et al.
International Journal of Molecular Medicine|November 15, 2016
Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic ricketsShan-Shan Li, Jie-Mei Gu, Wei-Jia Yu, et al.
Acta Pharmacologica Sinica|July 28, 2017
Association of bone turnover markers with glucose metabolism in Chinese populationJie Wang, Dan-Dan Yan, Xu-Hong Hou, et al.
Acta Pharmacologica Sinica|December 15, 2017
Association of serum uric acid levels with osteoporosis and bone turnover markers in a Chinese populationDan-Dan Yan, Jie Wang, Xu-Hong Hou, et al.
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