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Archives of Medical Research|October 15, 2013
Mutation screening for the EXT1 and EXT2 genes in Chinese patients with multiple osteochondromasQing-lin Kang, Jia Xu, Zeng Zhang, et al.
Journal of Bone and Mineral Metabolism|June 10, 2015
Two novel mutations of CLCN7 gene in Chinese families with autosomal dominant osteopetrosis (type II)Hui Zheng, Chong Shao, Yan Zheng, 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.
Biochemical and Biophysical Research Communications|June 21, 2012
Three novel PHEX gene mutations in four Chinese families with X-linked dominant hypophosphatemic ricketsQing-lin Kang, Jia Xu, Zeng Zhang, et al.
Acta Pharmacologica Sinica|June 7, 2016
BMP7 gene polymorphisms are not associated with bone mineral density or osteoporotic fractures in postmenopausal Chinese womenLi-Hong Gao, Shan-Shan Li, Chong Shao, et al.
Acta Pharmacologica Sinica|June 18, 2013
Association of serum 25-hydroxyvitamin D with insulin resistance and β-cell function in a healthy Chinese female populationMin-fang Tao, Zeng Zhang, Yao-hua Ke, et al.
Acta Pharmacologica Sinica|October 21, 2014
Serum osteocalcin levels are inversely associated with plasma glucose and body mass index in healthy Chinese womenWei-wei Hu, Yao-hua Ke, Jin-wei He, et al.
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