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Page 1
Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease.
Márquez-Ávila CS, Vizcaíno-Alarcón A, García-Delgado C, Núñez-Martínez PM, Flores-Ramírez F, Reyes-de la Rosa Adel P, Mendelsberg-Fishbein P, Ibarra-Grajeda D, Medina-Bravo P, Balderrábano-Saucedo N, Esteva-Solsona S, Márquez-Quiróz Ldel C, Flores-Cuevas A, Sánchez-Urbina R, Morales-Jiménez AB, Garibay-Nieto N, Del Bosque-Garza J, Pietropaolo-Cienfuegos D, Gutiérrez-Camacho C, García-Morales L, Morán-Barroso VF. Márquez-Ávila CS, et al. Int J Pediatr Otorhinolaryngol. 2015 Nov;79(11):1886-91. doi: 10.1016/j.ijporl.2015.08.038. Epub 2015 Sep 8. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26409294
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. 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
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. 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.
[Pallister-Killian syndrome in a Mexican mestizo patient. Case report].
Mendelsberg-Fishbein P, García-Delgado C, Muñoz-Martínez LB, Robledo-Cayetano M, Mejía-Marín LJ, Martínez-Barrera LE, Cerrillo-Hinojosa M, Moran-Barroso VF. Mendelsberg-Fishbein P, et al. Among authors: moran barroso vf. Arch Argent Pediatr. 2018 Feb 1;116(1):e135-e138. doi: 10.5546/aap.2018.e135. Arch Argent Pediatr. 2018. PMID: 29333839 Free article. Spanish.
[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: moran barroso vf. 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.
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.
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.
Caudal duplication with multicystic dysplastic kidney: a case report.
García-Delgado C, Mendelsberg-Fishbein P, González-Ledón F, Moreno-Salgado R, Blanco-Aguirre ME, Morán-Barroso VF. García-Delgado C, et al. Clin Dysmorphol. 2015 Jan;24(1):26-8. doi: 10.1097/MCD.0000000000000060. Clin Dysmorphol. 2015. PMID: 25304120 No abstract available.
32 results