APA (7th ed.) Citation

Moreno-Igoa, M., Hernández-Charro, B., Bengoa-Alonso, A., Pérez-Juana-del-Casal, A., Romero-Ibarra, C., Nieva-Echebarria, B., & Ramos-Arroyo, M. A. (2015). KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome. BMC Medical Genetics, 16(1), 1. https://doi.org/10.1186/s12881-015-0211-0

Chicago Style (17th ed.) Citation

Moreno-Igoa, María, Blanca Hernández-Charro, Amaya Bengoa-Alonso, Aranzazu Pérez-Juana-del-Casal, Carlos Romero-Ibarra, Beatriz Nieva-Echebarria, and María Antonia Ramos-Arroyo. "KANSL1 Gene Disruption Associated with the Full Clinical Spectrum of 17q21.31 Microdeletion Syndrome." BMC Medical Genetics 16, no. 1 (2015): 1. https://doi.org/10.1186/s12881-015-0211-0.

MLA (9th ed.) Citation

Moreno-Igoa, María, et al. "KANSL1 Gene Disruption Associated with the Full Clinical Spectrum of 17q21.31 Microdeletion Syndrome." BMC Medical Genetics, vol. 16, no. 1, 2015, p. 1, https://doi.org/10.1186/s12881-015-0211-0.