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Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing.
Matías-Pérez D, García-Montaño LA, Cruz-Aguilar M, García-Montalvo IA, Nava-Valdéz J, Barragán-Arevalo T, Villanueva-Mendoza C, Villarroel CE, Guadarrama-Vallejo C, la Cruz RV, Chacón-Camacho O, Zenteno JC. Matías-Pérez D, et al. Among authors: barragan arevalo t. J Hum Genet. 2018 Nov;63(11):1169-1180. doi: 10.1038/s10038-018-0504-1. Epub 2018 Sep 4. J Hum Genet. 2018. PMID: 30181649
Clinical characterization and identification of five novel FOXL2 pathogenic variants in a cohort of 12 Mexican subjects with the syndrome of blepharophimosis-ptosis-epicanthus inversus.
Chacón-Camacho OF, Salgado-Medina A, Alcaraz-Lares N, López-Moreno D, Barragán-Arévalo T, Nava-Castañeda A, Rodríguez-Uribe G, Lieberman E, Rodríguez-Cabrera L, González-Del Angel A, Borbolla AM, Fernández-Hernández L, Graue-Hernández EO, Zenteno JC. Chacón-Camacho OF, et al. Among authors: barragan arevalo t. Gene. 2019 Jul 20;706:62-68. doi: 10.1016/j.gene.2019.04.073. Epub 2019 Apr 29. Gene. 2019. PMID: 31048069
First Report of Mexican Patients with PACS1-Related Neurodevelopmental Disorder and Review of the PACS1-, PACS2-, and WDR37-Related Ophthalmological Manifestations.
Corona-Rivera JR, Zenteno JC, López-Pérez LG, Yokoyama-Rebollar E, Villarroel CE, Barragán-Arévalo T, Montes-Almanza LÁ, Zepeda-Romero LC, Morales-Domínguez GE, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Among authors: barragan arevalo t. Mol Syndromol. 2023 Apr;14(2):143-151. doi: 10.1159/000526975. Epub 2022 Dec 16. Mol Syndromol. 2023. PMID: 37064331 Free PMC article.
Lymphomatoid granulomatosis in a patient with DOCK8 deficiency.
Liquidano-Perez E, Alva-Chaire ADC, Yamazaki-Nakashimada MA, Pesantez Abril ÁA, Solorzano Morales SA, Ramírez Ristori AG, Barragán Arévalo T, Gonzalez-Serrano ME, Scheffler-Mendoza SC, Rodríguez-Jurado R. Liquidano-Perez E, et al. Among authors: barragan arevalo t. Pediatr Allergy Immunol. 2022 Jun;33(6):e13804. doi: 10.1111/pai.13804. Pediatr Allergy Immunol. 2022. PMID: 35754125 No abstract available.
[Combined immunodeficiency due to DOCK8 deficiency. State of the art].
Liquidano-Pérez E, Maza-Ramos G, Yamazaki-Nakashimada MA, Barragán-Arévalo T, Lugo-Reyes SO, Scheffler-Mendoza S, Espinosa-Padilla SE, González-Serrano ME. Liquidano-Pérez E, et al. Among authors: barragan arevalo t. Rev Alerg Mex. 2022 Jul 1;69(1):31-47. doi: 10.29262/ram.v69i1.1104. Rev Alerg Mex. 2022. PMID: 36927749 Spanish.
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