Order Article Reprints

Rutkowska L, Pinkier I, Sałacińska K, Kępczyński Ł, Salachna D, Lewek J, Banach M, Matusik P, Starostecka E, Lewiński A, et al. Identification of New Copy Number Variation and the Evaluation of a CNV Detection Tool for NGS Panel Data in Polish Familial Hypercholesterolemia Patients. Genes. 2022; 13(8):1424. https://doi.org/10.3390/genes13081424

Rutkowska, Lena, Iwona Pinkier, Kinga Sałacińska, Łukasz Kępczyński, Dominik Salachna, Joanna Lewek, Maciej Banach, Paweł Matusik, Ewa Starostecka, Andrzej Lewiński, and et al. 2022. "Identification of New Copy Number Variation and the Evaluation of a CNV Detection Tool for NGS Panel Data in Polish Familial Hypercholesterolemia Patients" Genes 13, no. 8: 1424. https://doi.org/10.3390/genes13081424

Rutkowska, L., Pinkier, I., Sałacińska, K., Kępczyński, Ł., Salachna, D., Lewek, J., Banach, M., Matusik, P., Starostecka, E., Lewiński, A., Płoski, R., Stawiński, P., & Gach, A. (2022). Identification of New Copy Number Variation and the Evaluation of a CNV Detection Tool for NGS Panel Data in Polish Familial Hypercholesterolemia Patients. Genes, 13(8), 1424. https://doi.org/10.3390/genes13081424