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Scientific Reports|June 29, 2017
Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean populationSangmoon Lee, Jihae Seo, Jinman Park, et al.
American Journal of Medical Genetics. Part A|July 14, 2016
Atypical presentation of infantile-onset farber disease with novel ASAH1 mutationsSoo Yeon Kim, Sun Ah Choi, Sangmoon Lee, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|September 5, 2015
Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC)Alexandre R Vieira, Moses Lee, Filippo Vairo, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 29, 2009
Genetic diagnosis by whole exome capture and massively parallel DNA sequencingMurim Choi, Ute I Scholl, Weizhen Ji, et al.
Science (New York, N.Y.)|August 28, 2010
Mitotic recombination in patients with ichthyosis causes reversion of dominant mutations in KRT10Keith A Choate, Yin Lu, Jing Zhou, et al.
Brain & Development|February 15, 2018
Diagnostic challenge for the rare lysosomal storage disease: Late infantile GM1 gangliosidosisJin Sook Lee, Jong-Moon Choi, Moses Lee, et al.
Experimental & Molecular Medicine|July 15, 2017
Findings of a 1303 Korean whole-exome sequencing studySoo Heon Kwak, Jeesoo Chae, Seongmin Choi, et al.
Experimental & Molecular Medicine|December 16, 2017
Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndromeHee Gyung Kang, Moses Lee, Kyoung Boon Lee, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|March 30, 2026
Conformable Microelectrode Arrays Integrated with a Scoop-Shaped Slide-Well for Dynamic Electrophysiological Profiling of Patient-Derived Cardiac OrganoidsYe Seul Kim, Jeonghwa Jeong, Gyeonghwa Heo, et al.
Journal of Virology|March 6, 2015
Increased Levels of Macrophage Inflammatory Proteins Result in Resistance to R5-Tropic HIV-1 in a Subset of Elite ControllersWendy E Walker, Sebastian Kurscheid, Samit Joshi, et al.
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