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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2005 2
2006 2
2007 2
2008 1
2009 1
2010 1
2011 1
2012 4
2013 2
2014 5
2015 6
2016 3
2017 1
2018 3
2019 2
2020 2
2022 1
2024 1

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37 results

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Page 1
Duplication of 12q24.21q24.33 in a Girl with Epilepsy, Expanding the Phenotype.
Plaza-Benhumea L, Martin-de Saro MD, Sanchez-Acosta CG, Messina-Baas O, Cuevas-Covarrubias SA. Plaza-Benhumea L, et al. Among authors: cuevas covarrubias sa. Mol Syndromol. 2022 Dec;13(5):409-418. doi: 10.1159/000521640. Epub 2022 Mar 10. Mol Syndromol. 2022. PMID: 36588755 Free PMC article.
New Genetic Variants of RUNX2 in Mexican Families Cause Cleidocranial Dysplasia.
Toral López J, Gómez Martinez S, Rivera Vega MDR, Hernández-Zamora E, Cuevas Covarrubias S, Ibarra Castrejón BA, González Huerta LM. Toral López J, et al. Among authors: cuevas covarrubias s. Biology (Basel). 2024 Mar 8;13(3):173. doi: 10.3390/biology13030173. Biology (Basel). 2024. PMID: 38534443 Free PMC article.
Gender-specific differences in clinical and metabolic variables associated with NAFLD in a Mexican pediatric population.
Villanueva-Ortega E, Garcés-Hernández MJ, Herrera-Rosas A, López-Alvarenga JC, Laresgoiti-Servitje E, Escobedo G, Queipo G, Cuevas-Covarrubias S, Garibay-Nieto GN. Villanueva-Ortega E, et al. Among authors: cuevas covarrubias s. Ann Hepatol. 2019 Sep-Oct;18(5):693-700. doi: 10.1016/j.aohep.2019.04.012. Epub 2019 May 22. Ann Hepatol. 2019. PMID: 31151875 Free article.
Whole sequence of the mitochondrial DNA genome of Kearns Sayre Syndrome patients: Identification of deletions and variants.
Saldaña-Martínez A, Muñoz ML, Pérez-Ramírez G, Montiel-Sosa JF, Montoya J, Emperador S, Ruiz-Pesini E, Cuevas-Covarrubias S, López-Valdez J, Ramírez RG. Saldaña-Martínez A, et al. Among authors: cuevas covarrubias s. Gene. 2019 Mar 10;688:171-181. doi: 10.1016/j.gene.2018.11.085. Epub 2018 Dec 5. Gene. 2019. PMID: 30528267
Two novel compound heterozygous families with a trimutation in the GJB2 gene causing sensorineural hearing loss.
Martínez-Saucedo M, Rivera-Vega Mdel R, Gonzalez--Huerta Luz M, Urueta-Cuellar H, Toral-López J, Berruecos-Villalobos P, Cuevas-Covarrubias S. Martínez-Saucedo M, et al. Among authors: cuevas covarrubias s. Int J Pediatr Otorhinolaryngol. 2015 Dec;79(12):2295-9. doi: 10.1016/j.ijporl.2015.10.030. Epub 2015 Oct 28. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26553399
Molecular characterization of Axenfeld-Rieger spectrum and other anterior segment dysgeneses in a sample of Mexican patients.
Hernández-Martínez N, González-Del Angel A, Alcántara-Ortigoza MA, González-Huerta LM, Cuevas-Covarrubias SA, Villanueva-Mendoza C. Hernández-Martínez N, et al. Among authors: cuevas covarrubias sa. Ophthalmic Genet. 2018 Dec;39(6):728-734. doi: 10.1080/13816810.2018.1547911. Epub 2018 Nov 20. Ophthalmic Genet. 2018. PMID: 30457409
37 results