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Acta Crystallographica. Section E, Structure Reports Online|November 18, 2011
2,5-Bis[2-(4-methyl-phen-yl)ethyn-yl]benzyl methacrylateZhen-Lin Zhang, Hai-Quan ZhangFrontiers in Genetics|August 2, 2021
Genotypic and Phenotypic Characteristics of 29 Patients With Rare Types of Osteogenesis Imperfecta: Average 5 Years of Follow-UpLei Xi, Hao Zhang, Zhen-Lin ZhangJournal of Bone and Mineral Metabolism|October 18, 2020
Clinical and genetic analysis in 185 Chinese probands of osteogenesis imperfectaLei Xi, Hao Zhang, Zhen-Lin ZhangBone|December 10, 2008
Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasiaHua Yue, Zhen-Lin Zhang, Jin-Wei HeEndocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|March 27, 2019
NOVEL MUTATIONS IN THE WNT1, TMEM38B, P4HB, AND PLS3 GENES IN FOUR UNRELATED CHINESE FAMILIES WITH OSTEOGENESIS IMPERFECTAYang-Jia Cao, Hao Zhang, Zhen-Lin ZhangNeuromuscular Disorders : NMD|April 8, 2018
A MYH3 mutation identified for the first time in a Chinese family with Sheldon-Hall syndrome (DA2B)Yang Xu, Qing-Lin Kang, Zhen-Lin ZhangMolecular Genetics & Genomic Medicine|April 5, 2021
Novel mutations in BMP1 result in a patient with autosomal recessive osteogenesis imperfectaLei Xi, Shanshan Lv, Hao Zhang, et al.Frontiers in Endocrinology|June 28, 2019
Expanding the Clinical Spectrum of Osteogenesis Imperfecta Type V: 13 Additional Patients and ReviewYang-Jia Cao, Zhe Wei, Hao Zhang, et al.Chinese Medical Journal|August 16, 2005
CMV-hFasL transgenic mice prevent from experimental autoimmune thyroiditisZhen-lin Zhang, Bo Lin, Lu-yang Yu, et al.Acta Pharmacologica Sinica|December 5, 2003
CMV-hFasL transgenic mice are sensitive to low doses of streptozotocin-induced type I diabetes mellitusBo Lin, Zhen-Lin Zhang, Lu-Yang Yu, et al.Pageof 13