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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2005 1
2007 3
2011 1
2012 1
2013 3
2014 1
2015 2
2016 6
2017 2
2018 5
2019 6
2020 5
2021 4
2022 3
2023 7
2024 3

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47 results

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Page 1
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.
Aneurysms involving the coronary arteries in a neonate with neurofibromatosis 1.
Corona-Rivera JR, Barrios-Prieto E, Rivera-Ramírez B, Sánchez-Uribe EH, Cortés-Pastrana RC, Aguilera CER, de Anda-Camacho RG, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Am J Med Genet A. 2023 Sep;191(9):2422-2427. doi: 10.1002/ajmg.a.63321. Epub 2023 Jun 6. Am J Med Genet A. 2023. PMID: 37278515 Review.
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. Among authors: corona rivera jr. 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
TRAPPC11-CDG muscular dystrophy: Review of 54 cases including a novel patient.
Corona-Rivera JR, Martínez-Duncker I, Morava E, Ranatunga W, Salinas-Marin R, González-Jaimes AM, Castillo-Reyes KA, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A, Orozco-Vela M, Brukman-Jiménez SA. Corona-Rivera JR, et al. Mol Genet Metab. 2024 May;142(1):108469. doi: 10.1016/j.ymgme.2024.108469. Epub 2024 Mar 28. Mol Genet Metab. 2024. PMID: 38564972 Review.
First Report of Mexican Patients with PACS1-Related Neurodevelopmental Disorder and Review of the PACS1-, PACS2-, and WDR37-Related Ophthalmological Manifestations.
Corona-Rivera JR, Zenteno JC, López-Pérez LG, Yokoyama-Rebollar E, Villarroel CE, Barragán-Arévalo T, Montes-Almanza LÁ, Zepeda-Romero LC, Morales-Domínguez GE, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A. Corona-Rivera JR, et al. Mol Syndromol. 2023 Apr;14(2):143-151. doi: 10.1159/000526975. Epub 2022 Dec 16. Mol Syndromol. 2023. PMID: 37064331 Free PMC article.
MTSS2-related neurodevelopmental disorder: Further delineation of the phenotype.
Corona-Rivera JR, Zenteno JC, Ordoñez-Labastida V, Cruz-Cruz JP, Cortés-Pastrana RC, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A, Martínez-Herrera A. Corona-Rivera JR, et al. Eur J Med Genet. 2023 Oct;66(10):104826. doi: 10.1016/j.ejmg.2023.104826. Epub 2023 Aug 30. Eur J Med Genet. 2023. PMID: 37657631
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. 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.
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.
47 results