Fragoso-Ontiveros, V., Velázquez-Aragón, J. A., Nuñez-Martínez, P. M., de la Luz Mejía-Aguayo, M., Vidal-Millán, S., Pedroza-Torres, A., . . . Alvarez-Gomez, R. M. (2019). Mexican BRCA1 founder mutation: Shortening the gap in genetic assessment for hereditary breast and ovarian cancer patients. PLoS One.
Citação norma ChicagoFragoso-Ontiveros, Veronica, et al. "Mexican BRCA1 Founder Mutation: Shortening the Gap in Genetic Assessment for Hereditary Breast and Ovarian Cancer Patients." PLoS One 2019.
MLA CitationFragoso-Ontiveros, Veronica, et al. "Mexican BRCA1 Founder Mutation: Shortening the Gap in Genetic Assessment for Hereditary Breast and Ovarian Cancer Patients." PLoS One 2019.
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