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Page 1
Analysis of the pathogenic variants of BRCA1 and BRCA2 using next-generation sequencing in women with familial breast cancer: a case-control study.
Zayas-Villanueva OA, Campos-Acevedo LD, Lugo-Trampe JJ, Hernández-Barajas D, González-Guerrero JF, Noriega-Iriondo MF, Ramírez-Sánchez IA, Martínez-de-Villarreal LE. Zayas-Villanueva OA, et al. BMC Cancer. 2019 Jul 22;19(1):722. doi: 10.1186/s12885-019-5950-4. BMC Cancer. 2019. PMID: 31331294 Free PMC article.
GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico.
Hernández-Juárez AA, Lugo-Trampe Jde J, Campos-Acevedo LD, Lugo-Trampe A, Treviño-González JL, de-la-Cruz-Ávila I, Martínez-de-Villarreal LE. Hernández-Juárez AA, et al. Int J Pediatr Otorhinolaryngol. 2014 Dec;78(12):2107-12. doi: 10.1016/j.ijporl.2014.09.016. Epub 2014 Sep 28. Int J Pediatr Otorhinolaryngol. 2014. PMID: 25288386
Detection of Turner Syndrome by quantitative PCR of SHOX and VAMP7 genes.
Ibarra-Ramírez M, Zamudio-Osuna MJ, Campos-Acevedo LD, Gallardo-Blanco HL, Cerda-Flores RM, Rodríguez-Sánchez IP, Martínez-de-Villarreal LE. Ibarra-Ramírez M, et al. Genet Test Mol Biomarkers. 2015 Feb;19(2):88-92. doi: 10.1089/gtmb.2014.0236. Epub 2014 Dec 23. Genet Test Mol Biomarkers. 2015. PMID: 25535777
Identification of novel mutations in Mexican patients with Aarskog-Scott syndrome.
Pérez-Coria M, Lugo-Trampe JJ, Zamudio-Osuna M, Rodríguez-Sánchez IP, Lugo-Trampe A, de la Fuente-Cortez B, Campos-Acevedo LD, Martínez-de-Villarreal LE. Pérez-Coria M, et al. Mol Genet Genomic Med. 2015 May;3(3):197-202. doi: 10.1002/mgg3.132. Epub 2015 Feb 17. Mol Genet Genomic Med. 2015. PMID: 26029706 Free PMC article.
Dosage of Sex Chromosomal Genes in Blood Deposited on Filter Paper for Neonatal Screening of Sex Chromosome Aneuploidy.
Campos-Acevedo LD, Ibarra-Ramirez M, de Jesús Lugo-Trampe J, de Jesús Zamudio-Osuna M, Torres-Muñoz I, Del Roble Velasco-Campos M, Rojas-Patlan L, Rodríguez-Sánchez IP, Martínez-de-Villarreal LE. Campos-Acevedo LD, et al. Genet Test Mol Biomarkers. 2016 Dec;20(12):786-790. doi: 10.1089/gtmb.2016.0101. Epub 2016 Oct 19. Genet Test Mol Biomarkers. 2016. PMID: 27997249
Bloom syndrome sans characteristic facial features in a Mestizo patient- a diagnostic challenge.
Chavez-Alvarez S, Villarreal-Martinez A, Velasco-Campos MDR, Moreno-Vega I, Martinez-de-Villarreal LE, Herz-Ruelas M, Ocampo-Candiani J, Campos-Acevedo LD. Chavez-Alvarez S, et al. Indian J Dermatol Venereol Leprol. 2019 Jan-Feb;85(1):130. doi: 10.4103/ijdvl.IJDVL_787_16. Indian J Dermatol Venereol Leprol. 2019. PMID: 29794356 Free article. No abstract available.
Genetic Variants in the 3'UTR of BRCA1 and BRCA2 Genes and their Putative Effects on the microRNA Mechanism in Hereditary Breast and Ovarian Cancer.
Sánchez-Chaparro MM, Garza-Veloz I, Zayas-Villanueva OA, Martinez-Fierro ML, Delgado-Enciso I, Gomez-Govea MA, Martínez-de-Villarreal LE, Reséndez-Pérez D, Rodríguez-Sánchez IP. Sánchez-Chaparro MM, et al. Diagnostics (Basel). 2020 May 13;10(5):298. doi: 10.3390/diagnostics10050298. Diagnostics (Basel). 2020. PMID: 32414209 Free PMC article.
Gene Copy Number Quantification of SHOX, VAMP7, and SRY for the Detection of Sex Chromosome Aneuploidies in Neonates.
Ibarra-Ramírez M, Lugo-Trampe JJ, Campos-Acevedo LD, Zamudio-Osuna M, Torres-Muñoz I, Gómez-Puente V, García-Castañeda G, Arredondo-Vázquez P, Rodríguez-Sánchez IP, Schaeffer SE, Velasco-Sepúlveda BH, Villarreal-Pérez JZ, Martínez-de-Villarreal LE. Ibarra-Ramírez M, et al. Genet Test Mol Biomarkers. 2020 Jun;24(6):352-358. doi: 10.1089/gtmb.2019.0226. Epub 2020 May 18. Genet Test Mol Biomarkers. 2020. PMID: 32423256
57 results