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Acta Pharmacologica Sinica|August 18, 2017
Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese familiesXiao-Ya Zhang, Jin-Wei He, Wen-Zhen Fu, et al.The Journal of Clinical Endocrinology and Metabolism|March 20, 2013
Mutations in the SLCO2A1 gene and primary hypertrophic osteoarthropathy: a clinical and biochemical characterizationZeng Zhang, Jin-Wei He, Wen-Zhen Fu, et al.Gene|March 28, 2013
A novel mutation in the SLCO2A1 gene in a Chinese family with primary hypertrophic osteoarthropathyZeng Zhang, Jin-Wei He, Wen-Zhen Fu, et al.Gene|November 5, 2013
Two novel mutations in the SLCO2A1 gene in a Chinese patient with primary hypertrophic osteoarthropathyZeng Zhang, Jin-Wei He, Wen-Zhen Fu, et al.Journal of Nutrigenetics and Nutrigenomics|December 22, 2016
Associations of Serum Osteocalcin and Polymorphisms of the Osteocalcin Gene with Bone Mineral Density in Postmenopausal and Elderly Chinese WomenXiao-Ya Zhang, Jin-Wei He, Wen-Zhen Fu, et al.Gene|October 3, 2012
Identification of one novel mutation in the EVC2 gene in a Chinese family with Ellis-van Creveld syndromeZeng Zhang, Kun Bao, Jin-Wei He, et al.Plos One|August 27, 2013
Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type VZeng Zhang, Mei Li, Jin-Wei He, et al.Acta Pharmacologica Sinica|March 7, 2019
Genetic variants in the PLS3 gene are associated with osteoporotic fractures in postmenopausal Chinese womenChong Shao, Yi-Wen Wang, Jin-Wei He, et al.Journal of Bone and Mineral Metabolism|May 14, 2020
Association between LGR4 polymorphisms and peak bone mineral density and body compositionWei-Jia Yu, Zeng Zhang, Wen-Zhen Fu, et al.Molecular Medicine Reports|July 20, 2016
Identification of two novel mutations in the COMP gene in six families with pseudoachondroplasiaWei-Jia Yu, Zeng Zhang, Jin-Wei He, et al.Pageof 6