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