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Arthritis & Rheumatology (Hoboken, N.J.)|June 28, 2022
Alterations of the Primary Cilia Gene SPAG17 and SOX9 Locus Noncoding RNAs Identified by RNA-Sequencing Analysis in Patients With Systemic SclerosisElisha D O Roberson, Mary Carns, Li Cao, et al.
Nature Communications|July 2, 2022
Photo-tailored heterocrystalline covalent organic framework membranes for organics separationJinqiu Yuan, Xinda You, Niaz Ali Khan, et al.
Seizure|December 5, 2020
Neurodevelopmental disorder caused by a truncating de novo variant of IRF2BPLXiao-Hang Qian, Xiao-Ying Liu, Ze-Yu Zhu, et al.
Neuromuscular Disorders : NMD|February 10, 2019
Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature reviewWo-Tu Tian, Xing-Hua Luan, Hai-Yan Zhou, et al.
Journal of Cardiovascular Computed Tomography|December 17, 2013
Congenital anomalies of coronary arteries in complex congenital heart disease: diagnosis and analysis with dual-source CTFang-fang Yu, Bin Lu, Yang Gao, et al.
Chemosphere|September 18, 2007
Contamination of soils with organochlorine pesticides in urban parks in Beijing, ChinaXing-hong Li, Wei Wang, Juan Wang, et al.
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