APA (7th ed.) Citation

Zodanu, G. K. E., Hwang, J. H., Mehta, Z., Sisniega, C., Barsegian, A., Kang, X., . . . 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

Chicago Style (17th ed.) Citation

Zodanu, Gloria K. E., et al. "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 (2024): 5469. https://doi.org/10.3390/ijms25105469.

MLA (9th ed.) Citation

Zodanu, Gloria K. E., et al. "High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects." International Journal of Molecular Sciences, vol. 25, no. 10, 2024, p. 5469, https://doi.org/10.3390/ijms25105469.