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.
Cita Chicago Style (17a ed.)León, Luis E., Felipe Benavides, Karena Espinoza, Cecilia Vial, Patricia Alvarez, Mirta Palomares, Guillermo Lay-Son, Macarena Miranda, y 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.
Cita MLA (8a ed.)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.