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Clinical insights from an unusual Turner syndrome manifestation: Congenital cutis verticis gyrata.
Corona-Rivera JR, Bustos Rodríguez FJ, Vega-Silva LL, Hernández-Camarena F, Peña-Padilla C, Castillo-Reyes KA, Cruz-Cruz JP, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Among authors: pena padilla c. Am J Med Genet A. 2023 Jun;191(6):1669-1671. doi: 10.1002/ajmg.a.63183. Epub 2023 Mar 18. Am J Med Genet A. 2023. PMID: 36932882 Review.
Aplasia cutis congenita of the scalp in a female infant with anophthalmia/microphthalmia-esophageal atresia syndrome negative for SOX2 mutation.
Corona-Rivera JR, Zenteno JC, Pelcastre-Luna E, Miguel-Jiménez K, Aguirre-Guillén RL, Cabral-Macías J, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Am J Med Genet A. 2013 May;161A(5):1189-93. doi: 10.1002/ajmg.a.35854. Epub 2013 Mar 5. Am J Med Genet A. 2013. PMID: 23463581 No abstract available.
Unusual retrospective prenatal findings in a male newborn with Timothy syndrome type 1.
Corona-Rivera JR, Barrios-Prieto E, Nieto-García R, Bloise R, Priori S, Napolitano C, Bobadilla-Morales L, Corona-Rivera A, Zapata-Aldana E, Peña-Padilla C, Rivera-Vargas J, Chavana-Naranjo E. Corona-Rivera JR, et al. Eur J Med Genet. 2015 Jun-Jul;58(6-7):332-5. doi: 10.1016/j.ejmg.2015.04.001. Epub 2015 Apr 13. Eur J Med Genet. 2015. PMID: 25882468
Oblique facial clefts in Johanson-Blizzard syndrome.
Corona-Rivera JR, Zapata-Aldana E, Bobadilla-Morales L, Corona-Rivera A, Peña-Padilla C, Solis-Hernández E, Guzmán C, Richmond E, Zahl C, Zenker M, Sukalo M. Corona-Rivera JR, et al. Am J Med Genet A. 2016 Jun;170(6):1495-501. doi: 10.1002/ajmg.a.37630. Epub 2016 Mar 17. Am J Med Genet A. 2016. PMID: 26989884 Review.
Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathy.
Peña-Padilla C, Marshall CR, Walker S, Scherer SW, Tavares-Macías G, Razo-Jiménez G, Bobadilla-Morales L, Acosta-Fernández E, Corona-Rivera A, Mendoza-Londono R, Corona-Rivera JR. Peña-Padilla C, et al. Clin Genet. 2017 Apr;91(4):640-646. doi: 10.1111/cge.12924. Epub 2017 Feb 16. Clin Genet. 2017. PMID: 27874174
Descriptive study of the complete blood count in newborn infants with Down syndrome.
Martínez-Macías FJ, Bobadilla-Morales L, González-Cruz J, Quiles-Corona M, Corona-Rivera A, Peña-Padilla C, Orozco-Vela M, Silva-Cruz R, Velarde-Rivera F, Corona-Rivera JR. Martínez-Macías FJ, et al. Am J Med Genet A. 2017 Apr;173(4):897-904. doi: 10.1002/ajmg.a.38097. Epub 2017 Feb 7. Am J Med Genet A. 2017. PMID: 28168815
Prevalence of orofacial clefts and risks for nonsyndromic cleft lip with or without cleft palate in newborns at a university hospital from West Mexico.
Corona-Rivera JR, Bobadilla-Morales L, Corona-Rivera A, Peña-Padilla C, Olvera-Molina S, Orozco-Martín MA, García-Cruz D, Ríos-Flores IM, Gómez-Rodríguez BG, Rivas-Soto G, Pérez-Molina JJ. Corona-Rivera JR, et al. Congenit Anom (Kyoto). 2018 Jul;58(4):117-123. doi: 10.1111/cga.12276. Epub 2018 Mar 4. Congenit Anom (Kyoto). 2018. PMID: 29457660
Pfeiffer Syndrome Type 3 and Prune Belly Anomaly in a Female: Case Report and Review.
Peña-Padilla C, Viramontes-Aguilar L, Tavares-Macías G, Bobadilla-Morales L, L Cunningham M, Park S, Zapata-Aldana E, Corona-Rivera JR. Peña-Padilla C, et al. Fetal Pediatr Pathol. 2019 Oct;38(5):412-417. doi: 10.1080/15513815.2019.1603256. Epub 2019 Apr 19. Fetal Pediatr Pathol. 2019. PMID: 31002276
30 results