Zodanu, G.K.E.; Hwang, J.H.; Mehta, Z.; Sisniega, C.; Barsegian, A.; Kang, X.; Biniwale, R.; Si, M.-S.; Satou, G.M.; Halnon, N.;
et al. High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects. Int. J. Mol. Sci. 2024, 25, 5469.
https://doi.org/10.3390/ijms25105469
AMA Style
Zodanu GKE, Hwang JH, Mehta Z, Sisniega C, Barsegian A, Kang X, Biniwale R, Si M-S, Satou GM, Halnon N,
et al. High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects. International Journal of Molecular Sciences. 2024; 25(10):5469.
https://doi.org/10.3390/ijms25105469
Chicago/Turabian Style
Zodanu, Gloria K. E., John H. Hwang, Zubin Mehta, Carlos Sisniega, Alexander Barsegian, Xuedong Kang, Reshma Biniwale, Ming-Sing Si, Gary M. Satou, Nancy Halnon,
and et al. 2024. "High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects" International Journal of Molecular Sciences 25, no. 10: 5469.
https://doi.org/10.3390/ijms25105469
APA Style
Zodanu, G. K. E., Hwang, J. H., Mehta, Z., Sisniega, C., Barsegian, A., Kang, X., Biniwale, R., Si, M. -S., Satou, G. M., Halnon, N., UCLA Congenital Heart Defect BioCore Faculty, Grody, W. W., Van Arsdell, G. S., Nelson, S. F., & Touma, M.
(2024). High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects. International Journal of Molecular Sciences, 25(10), 5469.
https://doi.org/10.3390/ijms25105469
