APA (7th ed.) Citation

León, L. E., Benavides, F., Espinoza, K., Vial, C., Alvarez, P., Palomares, M., . . . Repetto, G. M. (2017). Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients. Nature Portfolio.

Chicago Style (17th ed.) Citation

León, Luis E., Felipe Benavides, Karena Espinoza, Cecilia Vial, Patricia Alvarez, Mirta Palomares, Guillermo Lay-Son, Macarena Miranda, and Gabriela M. Repetto. Partial Microduplication in the Histone Acetyltransferase Complex Member KANSL1 Is Associated with Congenital Heart Defects in 22q11.2 Microdeletion Syndrome Patients. Nature Portfolio, 2017.

MLA (8th ed.) Citation

León, Luis E., et al. Partial Microduplication in the Histone Acetyltransferase Complex Member KANSL1 Is Associated with Congenital Heart Defects in 22q11.2 Microdeletion Syndrome Patients. Nature Portfolio, 2017.