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, 1424.
https://doi.org/10.3390/genes13081424
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
