Noonan syndrome: Severe phenotype and PTPN11 mutations.

MLA

Carrasco Salas, Pilar, et al. “Noonan Syndrome: Severe Phenotype and PTPN11 Mutations.” Medicina Clinica, vol. 152, no. 2, Jan. 2019, pp. 62–64. EBSCOhost, https://doi.org/10.1016/j.medcli.2018.03.015.

APA

Carrasco Salas, P., Gómez-Molina, G., Carreto-Alba, P., Granell-Escobar, R., Vázquez-Rico, I., & León-Justel, A. (2019). Noonan syndrome: Severe phenotype and PTPN11 mutations. Medicina Clinica, 152(2), 62–64. https://doi.org/10.1016/j.medcli.2018.03.015

Chicago

Carrasco Salas, Pilar, Gertrudis Gómez-Molina, Páxedes Carreto-Alba, Reyes Granell-Escobar, Ignacio Vázquez-Rico, and Antonio León-Justel. 2019. “Noonan Syndrome: Severe Phenotype and PTPN11 Mutations.” Medicina Clinica 152 (2): 62–64. doi:10.1016/j.medcli.2018.03.015.