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Hereditas|May 12, 2023
Whole-exome sequencing detected a novel AIFM1 variant in a Han-Chinese family with Cowchock syndromeChenyu Wang, Zhaojing Lin, ZhuangZhuang Yuan, et al.
Frontiers in Genetics|September 26, 2022
Novel heterozygous mutation in COL4A4 responsible for Alport syndrome in a Chinese familyRan Du, Jishi Liu, Yiqiao Hu, et al.
American Journal of Translational Research|July 26, 2021
Erratum: Use of whole-exome sequencing to identify a novel ADCY10 mutation in a patient with nephrolithiasisChenyu Wang, Ran Du, Jieyuan Jin, et al.
The Science of the Total Environment|November 3, 2023
Hydrothermal liquefaction of municipal sludge and its products applicationsYa Wei, Donghai Xu, Mingxin Xu, et al.
The Journal of Gene Medicine|September 24, 2021
CSRP3, p.Arg122*, is responsible for hypertrophic cardiomyopathy in a Chinese familyHao Huang, Yaqin Chen, Jieyuan Jin, et al.
Journal of the Chinese Medical Association : JCMA|August 7, 2024
Associated factors of osteoporosis in Chinese patients with rheumatoid arthritis: A systematic review and meta-analysisZhiming Song, Liangliang Fan, Hongyan Wang, et al.
Geriatric Nursing (New York, N.Y.)|July 12, 2024
Association between fear of falling and mortality in middle-aged and older adults: A systematic review and meta-analysisWenlian Ma, Xiaoli Liang, Hongyan Wang, et al.
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