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Clinical heterogeneity in Andersen-Tawil syndrome.
Totomoch-Serra A, Márquez MF, Cervantes-Barragan DE. Totomoch-Serra A, et al. Among authors: cervantes barragan de. Neuromuscul Disord. 2017 Nov;27(11):1074-1075. doi: 10.1016/j.nmd.2017.09.001. Epub 2017 Sep 14. Neuromuscul Disord. 2017. PMID: 29032928 No abstract available.
Setleis syndrome in Mexican-Nahua sibs due to a homozygous TWIST2 frameshift mutation and partial expression in heterozygotes: review of the focal facial dermal dysplasias and subtype reclassification.
Cervantes-Barragán DE, Villarroel CE, Medrano-Hernández A, Durán-McKinster C, Bosch-Canto V, Del-Castillo V, Nazarenko I, Yang A, Desnick RJ. Cervantes-Barragán DE, et al. J Med Genet. 2011 Oct;48(10):716-20. doi: 10.1136/jmedgenet-2011-100251. J Med Genet. 2011. PMID: 21931173
Newborn screening for six lysosomal storage disorders in a cohort of Mexican patients: Three-year findings from a screening program in a closed Mexican health system.
Navarrete-Martínez JI, Limón-Rojas AE, Gaytán-García MJ, Reyna-Figueroa J, Wakida-Kusunoki G, Delgado-Calvillo MDR, Cantú-Reyna C, Cruz-Camino H, Cervantes-Barragán DE. Navarrete-Martínez JI, et al. Among authors: cervantes barragan de. Mol Genet Metab. 2017 May;121(1):16-21. doi: 10.1016/j.ymgme.2017.03.001. Epub 2017 Mar 9. Mol Genet Metab. 2017. PMID: 28302345
Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations.
Salas-Labadía C, Gómez-Carmona S, Cruz-Alcívar R, Martínez-Anaya D, Del Castillo-Ruiz V, Durán-McKinster C, Ulloa-Avilés V, Yokoyama-Rebollar E, Ruiz-Herrera A, Navarrete-Meneses P, Lieberman-Hernández E, González-Del Angel A, Cervantes-Barragán D, Villarroel-Cortés C, Reyes-León A, Suárez-Pérez D, Pedraza-Meléndez A, González-Orsuna A, Pérez-Vera P. Salas-Labadía C, et al. Orphanet J Rare Dis. 2019 Nov 15;14(1):259. doi: 10.1186/s13023-019-1208-0. Orphanet J Rare Dis. 2019. PMID: 31730496 Free PMC article.
Mitochondrial DNA polymorphisms in Andersen-Tawil syndrome.
Totomoch-Serra A, Brito-Carreón CA, de L Muñoz M, Cervantes-Barragan D, Márquez MF. Totomoch-Serra A, et al. Kardiol Pol. 2020 Jun 25;78(6):581-583. doi: 10.33963/KP.15274. Epub 2020 Apr 2. Kardiol Pol. 2020. PMID: 32242403 Free article. No abstract available.
Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7.
Salas-Labadía C, Cervantes-Barragán DE, Cruz-Alcívar R, Daber RD, Conlin LK, Leonard LD, Spinner NB, Durán-McKinster C, Dávila-Ortíz de Montellano DJ, Del Castillo-Ruiz V, Pérez-Vera P. Salas-Labadía C, et al. Among authors: cervantes barragan de. Am J Med Genet A. 2014 Jul;164A(7):1765-9. doi: 10.1002/ajmg.a.36503. Epub 2014 Mar 26. Am J Med Genet A. 2014. PMID: 24677512 Review.
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