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Page 1
Mexican BRCA1 founder mutation: Shortening the gap in genetic assessment for hereditary breast and ovarian cancer patients.
Fragoso-Ontiveros V, Velázquez-Aragón JA, Nuñez-Martínez PM, de la Luz Mejía-Aguayo M, Vidal-Millán S, Pedroza-Torres A, Sánchez-Contreras Y, Ramírez-Otero MA, Muñiz-Mendoza R, Domínguez-Ortíz J, Wegman-Ostrosky T, Bargalló-Rocha JE, Gallardo-Rincón D, Reynoso-Noveron N, Arriaga-Canon C, Meneses-García A, Herrera-Montalvo LA, Alvarez-Gomez RM. Fragoso-Ontiveros V, et al. Among authors: nunez martinez pm. PLoS One. 2019 Sep 23;14(9):e0222709. doi: 10.1371/journal.pone.0222709. eCollection 2019. PLoS One. 2019. PMID: 31545835 Free PMC article.
A Previously Unrecognized Molecular Landscape of Lynch Syndrome in the Mexican Population.
Padua-Bracho A, Velázquez-Aragón JA, Fragoso-Ontiveros V, Nuñez-Martínez PM, Mejía Aguayo ML, Sánchez-Contreras Y, Ramirez-Otero MA, De la Fuente-Hernández MA, Vidal-Millán S, Wegman-Ostrosky T, Pedroza-Torres A, Arriaga-Canon C, Herrera-Montalvo LA, Alvarez-Gómez RM. Padua-Bracho A, et al. Among authors: nunez martinez pm. Int J Mol Sci. 2022 Sep 30;23(19):11549. doi: 10.3390/ijms231911549. Int J Mol Sci. 2022. PMID: 36232851 Free PMC article.
Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease.
Márquez-Ávila CS, Vizcaíno-Alarcón A, García-Delgado C, Núñez-Martínez PM, Flores-Ramírez F, Reyes-de la Rosa Adel P, Mendelsberg-Fishbein P, Ibarra-Grajeda D, Medina-Bravo P, Balderrábano-Saucedo N, Esteva-Solsona S, Márquez-Quiróz Ldel C, Flores-Cuevas A, Sánchez-Urbina R, Morales-Jiménez AB, Garibay-Nieto N, Del Bosque-Garza J, Pietropaolo-Cienfuegos D, Gutiérrez-Camacho C, García-Morales L, Morán-Barroso VF. Márquez-Ávila CS, et al. Among authors: nunez martinez pm. Int J Pediatr Otorhinolaryngol. 2015 Nov;79(11):1886-91. doi: 10.1016/j.ijporl.2015.08.038. Epub 2015 Sep 8. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26409294
A Molecular Characterization of the Allelic Expression of the BRCA1 Founder Δ9-12 Pathogenic Variant and Its Potential Clinical Relevance in Hereditary Cancer.
Dominguez-Ortiz J, Álvarez-Gómez RM, Montiel-Manríquez R, Cedro-Tanda A, Alcaraz N, Castro-Hernández C, Bautista-Hinojosa L, Contreras-Espinosa L, Torres-Maldonado L, Fragoso-Ontiveros V, Sánchez-Contreras Y, González-Barrios R, Fuente-Hernández MA, Mejía-Aguayo ML, Juárez-Figueroa U, Padua-Bracho A, Sosa-León R, Obregon-Serrano G, Vidal-Millán S, Núñez-Martínez PM, Pedroza-Torres A, Nicasio-Arzeta S, Rodríguez A, Luna F, Cisneros-Soberanis F, Frías S, Arriaga-Canon C, Herrera-Montalvo LA. Dominguez-Ortiz J, et al. Among authors: nunez martinez pm. Int J Mol Sci. 2024 Jun 20;25(12):6773. doi: 10.3390/ijms25126773. Int J Mol Sci. 2024. PMID: 38928478 Free PMC article.