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Journal of Pediatric Endocrinology & Metabolism : JPEM|January 14, 2020
Familial hypophosphatemic rickets caused by a PHEX gene mutation accompanied by a NPR2 missense mutationYongting Zhao, Fan Yang, Lihong Wang, et al.
Sensors (Basel, Switzerland)|January 30, 2021
Non-Communication Decentralized Multi-Robot Collision Avoidance in Grid Map Workspace with Double Deep Q-NetworkLin Chen, Yongting Zhao, Huanjun Zhao, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|October 26, 2019
A novel heterozygous intron mutation in SEMA7A causing kallmann syndrome in a femaleYongting Zhao, Fan Yang, Lili Qiu, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|January 8, 2019
A new compound heterozygous mutation in a female with 17α-hydroxylase/17,20-lyase deficiency, slipped capital femoral epiphysis, and adrenal myelolipomaFan Yang, Yongting Zhao, Jie Lv, et al.
Acta Pharmaceutica Sinica. B|February 7, 2022
Preliminary evidence for the presence of multiple forms of cell death in diabetes cardiomyopathyJinjing Wei, Yongting Zhao, Haihai Liang, et al.
Frontiers in Endocrinology|January 30, 2023
Differentially expressed tRNA-derived fragments and their roles in primary cardiomyocytes stimulated by high glucoseYongting Zhao, Ruxin Wang, Qi Qin, et al.
Journal of Oleo Science|May 2, 2017
Biodiesel Production by Catalytic Esterification of Oleic Acid over Copper (II)-Alginate ComplexesQiuyun Zhang, Fangfang Wei, Yutao Zhang, et al.
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