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Page 1
X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient.
Noriega-Juárez MA, García-Delgado C, Villaseñor-Domínguez A, Mena-Cedillos CA, Toledo-Bahena M, Valencia-Herrera A, Baeza-Capetillo P, Cervantes A, Morán-Barroso VF, Monroy-Jaramillo N. Noriega-Juárez MA, et al. Among authors: cervantes a. Bol Med Hosp Infant Mex. 2020;77(4):212-217. doi: 10.24875/BMHIM.19000209. Bol Med Hosp Infant Mex. 2020. PMID: 32713954 English.
Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia.
Monroy-Jaramillo N, Abad-Flores JD, García-Delgado C, Villaseñor-Domínguez A, Mena-Cedillos C, Toledo-Bahena ME, Valencia-Herrera AM, Sánchez-Boiso A, Akaki-Carreño YI, Del Río Navarro B, Aguirre-Hernández J, López-López M, Cervantes A, Cerbón M, Morán-Barroso VF. Monroy-Jaramillo N, et al. Among authors: cervantes a. J Eur Acad Dermatol Venereol. 2017 Jul;31(7):e321-e324. doi: 10.1111/jdv.14107. Epub 2017 Feb 17. J Eur Acad Dermatol Venereol. 2017. PMID: 28045201 No abstract available.
Congenital hypertrichosis universalis in Mexican female twins.
Cervantes A, García-Delgado C, Fernández-Ramírez F, Valencia-Herrera A, Kofman S, Morán-Barroso V. Cervantes A, et al. Int J Dermatol. 2016 Jan;55(1):e29-31. doi: 10.1111/ijd.13104. Epub 2015 Oct 30. Int J Dermatol. 2016. PMID: 26518157 Review. No abstract available.
Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population.
Cerón-Rodríguez M, Vázquez-Martínez ER, García-Delgado C, Ortega-Vázquez A, Valencia-Mayoral P, Ramírez-Devars L, Arias-Villegas C, Monroy-Muñoz IE, López M, Cervantes A, Cerbón M, Morán-Barroso VF. Cerón-Rodríguez M, et al. Among authors: cervantes a. Ann Hepatol. 2019 Jul-Aug;18(4):613-619. doi: 10.1016/j.aohep.2018.12.004. Epub 2019 May 12. Ann Hepatol. 2019. PMID: 31122880 Free article.
Cytogenetic profile in 1,921 cases of trisomy 21 syndrome.
Flores-Ramírez F, Palacios-Guerrero C, García-Delgado C, Morales-Jiménez AB, Arias-Villegas CM, Cervantes A, Morán-Barroso VF. Flores-Ramírez F, et al. Among authors: cervantes a. Arch Med Res. 2015 Aug;46(6):484-9. doi: 10.1016/j.arcmed.2015.08.001. Epub 2015 Aug 24. Arch Med Res. 2015. PMID: 26314225
[Monosomy 9p24 in two non-related patients as result of a translocation (2;9)].
León-Carlos NY, García-Delgado C, Morales-Jiménez AB, Serrano-Bello C, Cervantes A, Morán Barroso VF. León-Carlos NY, et al. Among authors: cervantes a. Arch Argent Pediatr. 2018 Aug 1;116(4):e603-e608. doi: 10.5546/aap.2018.e603. Arch Argent Pediatr. 2018. PMID: 30016040 Free article. Spanish.
Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
Cervantes A, García-Delgado C, Fernández-Ramírez F, Galaz-Montoya C, Morales-Jiménez AB, Nieto-Martínez K, Gómez-Laguna L, Villa-Morales J, Quintana-Palma M, Berúmen J, Kofman S, Morán-Barroso VF. Cervantes A, et al. BMC Med Genomics. 2014 Sep 15;7:55. doi: 10.1186/1755-8794-7-55. BMC Med Genomics. 2014. PMID: 25223409 Free PMC article.
Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event.
Morán-Barroso VF, Cervantes A, Rivera-Vega MDR, Del Castillo-Moreno A, Moreno-Chacón A, Mejía-Cauich E, Contreras-Ortiz LE, Fernández-Ramírez F. Morán-Barroso VF, et al. Among authors: cervantes a. Mol Genet Genomic Med. 2021 Sep;9(9):e1762. doi: 10.1002/mgg3.1762. Epub 2021 Jul 20. Mol Genet Genomic Med. 2021. PMID: 34288579 Free PMC article.
Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.
Gómez-Laguna L, Martínez-Herrera A, Reyes-de la Rosa ADP, García-Delgado C, Nieto-Martínez K, Fernández-Ramírez F, Valderrama-Atayupanqui TY, Morales-Jiménez AB, Villa-Morales J, Kofman S, Cervantes A, Morán-Barroso VF. Gómez-Laguna L, et al. Among authors: cervantes a. Ophthalmic Genet. 2018 Jan-Feb;39(1):56-62. doi: 10.1080/13816810.2017.1363245. Epub 2017 Sep 18. Ophthalmic Genet. 2018. PMID: 28922055 Review.
Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.
Abreu-González M, García-Delgado C, Cervantes A, Aparicio-Onofre A, Guevara-Yáñez R, Sánchez-Urbina R, Gallegos-Arreola MP, Luna-Angulo A, Estrada FJ, Morán-Barroso VF. Abreu-González M, et al. Among authors: cervantes a. Case Rep Genet. 2013;2013:895259. doi: 10.1155/2013/895259. Epub 2013 Sep 18. Case Rep Genet. 2013. PMID: 24151567 Free PMC article.
608 results