Santos, M., Temudo, T., Kay, T., Carrilho, I., Medeira, A., Cabral, H., . . . Maciel, P. (2009). Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients.
Citação norma ChicagoSantos, Mónica, et al. Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-like or Related Neurodevelopmental Phenotype in Male Patients. 2009.
Citação norma MLASantos, Mónica, et al. Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-like or Related Neurodevelopmental Phenotype in Male Patients. 2009.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.