Showing results (11-20 of 124) with videos related to
Sort By:
Pageof 13
The Journal of Dermatology|April 4, 2018
Cutis laxa in a patient with 1p36 deletion syndromeZhen Zhang, Jian Wang, Niu Li, et al.Experimental and Therapeutic Medicine|June 8, 2017
Novel variant in the FGD1 gene causing Aarskog-Scott syndromeYihua Ge, Niu Li, Zhigang Wang, et al.BMC Pregnancy and Childbirth|July 2, 2024
Concurrent of compound heterozygous variant of a novel in-frame deletion and the common hypomorphic haplotype in TBX6 and inherited 17q12 microdeletion in a fetusGuoqiang Li, Yiyao Chen, Xu Han, et al.Ultrasonics Sonochemistry|September 12, 2007
Synthesis of MCM-22 zeolite by an ultrasonic-assisted aging procedureBaoyu Wang, Jianmei Wu, Zhong-Yong Yuan, et al.Physical Review Letters|August 20, 2016
Probing Resonances of the Dirac Equation with Complex Momentum RepresentationNiu Li, Min Shi, Jian-You Guo, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 6, 2023
Defective Joint Development and Maintenance in GDF6-Related Multiple Synostoses SyndromeTingting Yu, Guoqiang Li, Chen Wang, et al.Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|December 18, 2023
Autosomal dominant neurodevelopmental disorders associated with KIF1A gene variants in 6 pediatric patientsJingqi Lin, Niu Li, Ru'en Yao, et al.Cytokine|September 1, 2018
The association between sixteen genome-wide association studies-related allergic diseases loci and childhood allergic rhinitis in a Chinese Han populationYoujin Li, Jie Chen, Xiaoqing Rui, et al.British Journal of Haematology|July 29, 2025
Alu-mediated FANCD2 exonic deletion contributes to Fanconi anaemiaShaofang Shangguan, Xinyuan Cui, Juanjuan Li, et al.The Science of the Total Environment|July 29, 2024
Thinning alters nitrogen transformation processes in subtropical forest soil: Key roles of physicochemical propertiesLiangjin Yao, Chuping Wu, Bo Jiang, et al.Pageof 13