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Tilemis F-N, Marinakis NM, Veltra D, Svingou M, Kekou K, Mitrakos A, Tzetis M, Kosma K, Makrythanasis P, Traeger-Synodinos J, et al. Germline CNV Detection through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases. Genes. 2023; 14(7):1490. https://doi.org/10.3390/genes14071490

Tilemis, Faidon-Nikolaos, Nikolaos M. Marinakis, Danai Veltra, Maria Svingou, Kyriaki Kekou, Anastasios Mitrakos, Maria Tzetis, Konstantina Kosma, Periklis Makrythanasis, Joanne Traeger-Synodinos, and et al. 2023. "Germline CNV Detection through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases" Genes 14, no. 7: 1490. https://doi.org/10.3390/genes14071490

Tilemis, F.-N., Marinakis, N. M., Veltra, D., Svingou, M., Kekou, K., Mitrakos, A., Tzetis, M., Kosma, K., Makrythanasis, P., Traeger-Synodinos, J., & Sofocleous, C. (2023). Germline CNV Detection through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases. Genes, 14(7), 1490. https://doi.org/10.3390/genes14071490