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Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation.
Acosta-Fernández E, Zenteno JC, Chacón-Camacho OF, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A, Romo-Huerta CO, Zepeda-Romero LC, López-Marure E, Acosta-León J, García-Cruz D, Maciel-Cruz EJ, Corona-Rivera JR. Acosta-Fernández E, et al. Among authors: zepeda romero lc. Am J Med Genet A. 2020 May;182(5):1223-1229. doi: 10.1002/ajmg.a.61506. Epub 2020 Feb 5. Am J Med Genet A. 2020. PMID: 32022998
Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes.
Corona-Rivera JR, Corona-Rivera A, Zepeda-Romero LC, Rios-Flores IM, Rivera-Vargas J, Orozco-Vela M, Santana-Bejarano UF, Torres-Anguiano E, Pinto-Cardoso M, David D, Bobadilla-Morales L. Corona-Rivera JR, et al. Among authors: zepeda romero lc. Congenit Anom (Kyoto). 2019 Sep;59(5):174-178. doi: 10.1111/cga.12309. Epub 2018 Oct 9. Congenit Anom (Kyoto). 2019. PMID: 30225942 Review.
Clinical characteristics and functional outcome of pediatric ocular trauma in a third level reference hospital in Guadalajara, Mexico.
Zepeda-Romero LC, Saucedo-Rodríguez LR, Becerra-Cota M, Gutiérrez-Padilla JA, Yanowsky-Reyes G, Pérez-Rulfo-Ibarra D, Díaz-Borrayo N, Cabrera-Díaz NN, Barrera-de-León JC. Zepeda-Romero LC, et al. Bol Med Hosp Infant Mex. 2022;79(1):26-32. doi: 10.24875/BMHIM.21000077. Bol Med Hosp Infant Mex. 2022. PMID: 35086126 Free article. English.
Early retinopathy of prematurity findings identified with fluorescein angiography.
Zepeda-Romero LC, Oregon-Miranda AA, Lizarraga-Barrón DS, Gutiérrez-Camarena O, Meza-Anguiano A, Gutiérrez-Padilla JA. Zepeda-Romero LC, et al. Graefes Arch Clin Exp Ophthalmol. 2013 Sep;251(9):2093-7. doi: 10.1007/s00417-013-2321-8. Epub 2013 Apr 2. Graefes Arch Clin Exp Ophthalmol. 2013. PMID: 23546400
24 results