Komlósi, K., Duga, B., Hadzsiev, K., Czakó, M., Kosztolányi, G., Fogarasi, A., & Melegh, B. (2015). Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome. Molecular Cytogenetics (17558166), 8(1), 1. https://doi.org/10.1186/s13039-015-0118-7
Chicago Style (17th ed.) CitationKomlósi, Katalin, Balázs Duga, Kinga Hadzsiev, Márta Czakó, György Kosztolányi, András Fogarasi, and Béla Melegh. "Phenotypic Variability in a Hungarian Patient with the 4q21 Microdeletion Syndrome." Molecular Cytogenetics (17558166) 8, no. 1 (2015): 1. https://doi.org/10.1186/s13039-015-0118-7.
MLA (9th ed.) CitationKomlósi, Katalin, et al. "Phenotypic Variability in a Hungarian Patient with the 4q21 Microdeletion Syndrome." Molecular Cytogenetics (17558166), vol. 8, no. 1, 2015, p. 1, https://doi.org/10.1186/s13039-015-0118-7.