MAM, D., J, Y., CM, W., M, M., SM, B., CF, I., & C, T. (2026). Diagnostic discovery of structural variants causing foveal hypoplasia using SVRare and long-read nanopore sequencing. European journal of human genetics : EJHG, 34(10), 1493. https://doi.org/10.1038/s41431-026-02190-y
Παραπομπή σε μορφή Chicago (17η εκδ.)MAM, Derar, Yu J, Watson CM, McKibbin M, Bell SM, Inglehearn CF, και Toomes C. "Diagnostic Discovery of Structural Variants Causing Foveal Hypoplasia Using SVRare and Long-read Nanopore Sequencing." European Journal of Human Genetics : EJHG 34, no. 10 (2026): 1493. https://doi.org/10.1038/s41431-026-02190-y.
Παραπομπή σε μορφή MLA (9th εκδ.)MAM, Derar, et al. "Diagnostic Discovery of Structural Variants Causing Foveal Hypoplasia Using SVRare and Long-read Nanopore Sequencing." European Journal of Human Genetics : EJHG, vol. 34, no. 10, 2026, p. 1493, https://doi.org/10.1038/s41431-026-02190-y.