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Experimental Hematology|July 22, 2018
Functional analysis of Fanconi anemia mutations in ChinaNiu Li, Lixia Ding, Benshang Li, et al.
Nucleic Acids Research|January 26, 2020
Cooperation of the NEIL3 and Fanconi anemia/BRCA pathways in interstrand crosslink repairNiu Li, Jian Wang, Susan S Wallace, et al.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University|August 21, 2019
Exploration of susceptible genes associated with Henoch-Schönlein purpura by whole exome sequencingYanliang Jin, Qiuling Xie, Niu Li, et al.
Fetal and Pediatric Pathology|April 21, 2017
De Novo Mutation of KAT6B Gene Causing Atypical Say-Barber-Biesecker-Young-Simpson Syndrome or Genitopatellar SyndromeGuoqiang Li, Niu Li, Juan Li, et al.
Brazilian Journal of Otorhinolaryngology|April 12, 2025
Diagnosis of a patient with severe sensorineural hearing loss as the initial symptom caused by novel compound heterozygous variant in SLA19A2 geneYanan Shi, Junyang Li, Xiaoqin Chen, et al.
Zhongguo Zhen Jiu = Chinese Acupuncture & Moxibustion|May 18, 2023
[Acupuncture with Tiaochong Shugan method by stages for menstrual headache based on syndrome differentiation: a randomized controlled trial]Jin-Niu Li, Jia Li, Jie Liu, et al.
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