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Nonmosaic Trisomy 19p13.3p13.2 Resulting from a Rare Unbalanced t(Y;19)(q12;p13.2) Translocation in a Patient with Pachygyria and Polymicrogyria.
Martínez Anaya D, Fernández Hernández L, González Del Angel A, Alcántara Ortigoza MA, Ulloa Avilés V, Pérez Vera P. Martínez Anaya D, et al. Among authors: gonzalez del angel a. Cytogenet Genome Res. 2020;160(4):177-184. doi: 10.1159/000507561. Epub 2020 May 6. Cytogenet Genome Res. 2020. PMID: 32369810
Association of interactions among the IRF6 gene, the 8q24 region, and maternal folic acid intake with non-syndromic cleft lip/palate in Mexican Mestizos.
Velázquez-Aragón JA, Alcántara-Ortigoza MA, Estandia-Ortega B, Reyna-Fabián ME, Cruz-Fuentes C, Villagómez S, González-del Angel A. Velázquez-Aragón JA, et al. Among authors: gonzalez del angel a. Am J Med Genet A. 2012 Dec;158A(12):3207-10. doi: 10.1002/ajmg.a.35641. Epub 2012 Nov 20. Am J Med Genet A. 2012. PMID: 23169698 No abstract available.
5,10-Methylenetetrahydrofolate reductase single nucleotide polymorphisms and gene-environment interaction analysis in non-syndromic cleft lip/palate.
Estandia-Ortega B, Velázquez-Aragón JA, Alcántara-Ortigoza MA, Reyna-Fabian ME, Villagómez-Martínez S, González-Del Angel A. Estandia-Ortega B, et al. Among authors: gonzalez del angel a. Eur J Oral Sci. 2014 Apr;122(2):109-13. doi: 10.1111/eos.12114. Epub 2014 Jan 24. Eur J Oral Sci. 2014. PMID: 24460828
Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects.
Alcántara-Ortigoza MA, De Rubens-Figueroa J, Reyna-Fabian ME, Estandía-Ortega B, González-del Angel A, Molina-Álvarez B, Velázquez-Aragón JA, Villagómez-Martínez S, Pereira-López GI, Martínez-Cruz V, Álvarez-Gómez RM, Díaz-García L. Alcántara-Ortigoza MA, et al. Among authors: gonzalez del angel a. Pediatr Cardiol. 2015 Apr;36(4):802-8. doi: 10.1007/s00246-014-1091-3. Epub 2014 Dec 19. Pediatr Cardiol. 2015. PMID: 25524324
Wide allelic heterogeneity with predominance of large IDS gene complex rearrangements in a sample of Mexican patients with Hunter syndrome.
Alcántara-Ortigoza MA, García-de Teresa B, González-Del Angel A, Berumen J, Guardado-Estrada M, Fernández-Hernández L, Navarrete-Martínez JI, Maza-Morales M, Rius-Domínguez R. Alcántara-Ortigoza MA, et al. Among authors: gonzalez del angel a. Clin Genet. 2016 May;89(5):574-83. doi: 10.1111/cge.12738. Epub 2016 Feb 9. Clin Genet. 2016. PMID: 26762690
An uncommon inheritance pattern in Niemann-Pick disease type C: identification of probable paternal germline mosaicism in a Mexican family.
Cervera-Gaviria M, Alcántara-Ortigoza MA, González-Del Angel A, Moyers-Pérez P, Legorreta-Ramírez BG, Barrera-Carmona N, Cervera-Gaviria J. Cervera-Gaviria M, et al. Among authors: gonzalez del angel a. BMC Neurol. 2016 Aug 22;16(1):147. doi: 10.1186/s12883-016-0649-5. BMC Neurol. 2016. PMID: 27549128 Free PMC article.
75 results