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Complete blood count differences in a cohort of Down syndrome neonates with transient abnormal myelopoiesis screened for GATA1 pathogenic variants.
Am J Med Genet A. 2020 Sep;182(9):2085-2093. doi: 10.1002/ajmg.a.61748. Epub 2020 Jul 18.
Am J Med Genet A. 2020.
PMID: 32681702
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. Among authors: orozco vela m.
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
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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: orozco vela m.
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.
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Prevalence and risk factors for Down syndrome: A hospital-based single-center study in Western Mexico.
Corona-Rivera JR, Martínez-Macías FJ, Bobadilla-Morales L, Corona-Rivera A, Peña-Padilla C, Rios-Flores IM, Flores-Guevara PA, Orozco-Vela M, Aranda-Sánchez CI, Brukman-Jiménez SA.
Corona-Rivera JR, et al. Among authors: orozco vela m.
Am J Med Genet A. 2019 Mar;179(3):435-441. doi: 10.1002/ajmg.a.61044. Epub 2019 Jan 21.
Am J Med Genet A. 2019.
PMID: 30666778
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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. Among authors: orozco vela m.
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.
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MTHFR 677C>T and 1298A>C Variants in Mothers of Infants with Down Syndrome from Western Mexico.
Romero-Bolaño YM, Bobadilla-Morales L, Corona-Rivera A, Cuero-Quezada I, Santana-Hernández J, Peña-Padilla C, Brukman-Jiménez A, Orozco-Vela M, Navia-Espinoza N, Corona-Rivera JR.
Romero-Bolaño YM, et al. Among authors: orozco vela m.
Genet Test Mol Biomarkers. 2024 May 8. doi: 10.1089/gtmb.2023.0690. Online ahead of print.
Genet Test Mol Biomarkers. 2024.
PMID: 38717090
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