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Broadening the spectrum of Catania brachydactylous type of acrofacial dysostoses.
Aguirre-Guillén RL, Santoyo-Duran R, Tapia-Hernández R, González-Bernal C, Tostado-Rabago EA, Díaz-Silva M, Valero-Rodríguez DL, Mellín-Sánchez EL, Corona-Rivera JR. Aguirre-Guillén RL, et al. Clin Dysmorphol. 2015 Oct;24(4):163-5. doi: 10.1097/MCD.0000000000000089. Clin Dysmorphol. 2015. PMID: 25945454 No abstract available.
Agenesis of the vocal cords in a female infant with Robin sequence.
Corona-Rivera JR, Yanowsky-Reyes G, Arnaud-López L, Bobadilla-Morales L, Aguirre-Guillén RL, Jasso-Bernal JE, Corona-Rivera A, Aguirre-Jáuregui O. Corona-Rivera JR, et al. Clin Dysmorphol. 2011 Oct;20(4):232-233. doi: 10.1097/MCD.0b013e328347bf41. Clin Dysmorphol. 2011. PMID: 21629115 No abstract available.
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.
Associated congenital anomalies in infants with isolated gastroschisis: A single-institutional experience.
Corona-Rivera JR, Nieto-García R, López-Marure E, Cárdenas-Ruiz Velasco JJ, Bobadilla-Morales L, Mellín-Sánchez EL, Aguirre-Guillén RL, Pérez-Ramírez RO, Zapata-Aldana E, Sandoval-Talamantes AK, Solís-Ledezma S, Corona-Rivera A, Gómez-Ruiz LM. Corona-Rivera JR, et al. Am J Med Genet A. 2016 Feb;170A(2):316-321. doi: 10.1002/ajmg.a.37433. Epub 2015 Oct 14. Am J Med Genet A. 2016. PMID: 26464049 Clinical Trial.
Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome.
Zepeda-Romero LC, Zenker M, Schanze D, Schanze I, Peña-Padilla C, Quezada-Salazar CA, Pacheco-Torres PA, Rivera-Montellano ML, Aguirre-Guillén RL, Bobadilla-Morales L, Corona-Rivera A, Corona-Rivera JR. Zepeda-Romero LC, et al. Eur J Med Genet. 2022 Dec;65(12):104653. doi: 10.1016/j.ejmg.2022.104653. Epub 2022 Oct 28. Eur J Med Genet. 2022. PMID: 36330903
Intrafamilial variability and neurological manifestations in two siblings with carbohydrate sulfotransferase 3-related skeletal dysplasia.
Rivera-Vargas J, Superti-Furga A, Bonafé L, Peña-Padilla C, Cortés-Pastrana RC, Bobadilla-Morales L, Corona-Rivera A, Corona-Rivera JR. Rivera-Vargas J, et al. Among authors: corona rivera jr. Clin Dysmorphol. 2023 Jan 1;32(1):14-17. doi: 10.1097/MCD.0000000000000432. Epub 2022 Sep 12. Clin Dysmorphol. 2023. PMID: 36503918 No abstract available.
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
80 results