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High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.
Zodanu GKE, Hwang JH, Mehta Z, Sisniega C, Barsegian A, Kang X, Biniwale R, Si MS, Satou GM, Halnon N, Ucla Congenital Heart Defect BioCore Faculty, Grody WW, Van Arsdell GS, Nelson SF, Touma M. Zodanu GKE, et al. Among authors: hwang jh. Int J Mol Sci. 2024 May 17;25(10):5469. doi: 10.3390/ijms25105469. Int J Mol Sci. 2024. PMID: 38791509
Strain-invariant stretchable radio-frequency electronics.
Kim SH, Basir A, Avila R, Lim J, Hong SW, Choe G, Shin JH, Hwang JH, Park SY, Joo J, Lee C, Choi J, Lee B, Choi KS, Jung S, Kim TI, Yoo H, Jung YH. Kim SH, et al. Among authors: hwang jh. Nature. 2024 May 22. doi: 10.1038/s41586-024-07383-3. Online ahead of print. Nature. 2024. PMID: 38778108
2,242 results