Order Article Reprints

Moustakli E, Christopoulos P, Potiris A, Zikopoulos A, Mavrogianni D, Karampas G, Kathopoulis N, Anagnostaki I, Domali E, Tzallas AT, et al. Long-Read Sequencing and Structural Variant Detection: Unlocking the Hidden Genome in Rare Genetic Disorders. Diagnostics. 2025; 15(14):1803. https://doi.org/10.3390/diagnostics15141803

Moustakli, Efthalia, Panagiotis Christopoulos, Anastasios Potiris, Athanasios Zikopoulos, Despoina Mavrogianni, Grigorios Karampas, Nikolaos Kathopoulis, Ismini Anagnostaki, Ekaterini Domali, Alexandros T. Tzallas, and et al. 2025. "Long-Read Sequencing and Structural Variant Detection: Unlocking the Hidden Genome in Rare Genetic Disorders" Diagnostics 15, no. 14: 1803. https://doi.org/10.3390/diagnostics15141803

Moustakli, E., Christopoulos, P., Potiris, A., Zikopoulos, A., Mavrogianni, D., Karampas, G., Kathopoulis, N., Anagnostaki, I., Domali, E., Tzallas, A. T., Drakakis, P., & Stavros, S. (2025). Long-Read Sequencing and Structural Variant Detection: Unlocking the Hidden Genome in Rare Genetic Disorders. Diagnostics, 15(14), 1803. https://doi.org/10.3390/diagnostics15141803