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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: rivera vargas j. 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.
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. Among authors: rivera vargas j. 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
Aneuploidy identification in pre-B acute lymphoblastic leukemia patients at diagnosis by Multiplex Ligation-dependent Probe Amplification (MLPA).
Vázquez-Reyes A, Bobadilla-Morales L, Barba-Barba C, Macías-Salcedo G, Serafín-Saucedo G, Velázquez-Rivera ME, Almodóvar-Cuevas MC, Márquez-Mora A, Pimentel-Gutiérrez HJ, Ortega-de-la-Torre C, Cruz-Osorio RM, Nava-Gervasio S, Rivera-Vargas J, Sánchez-Zubieta F, Corona-Rivera JR, Corona-Rivera A. Vázquez-Reyes A, et al. Among authors: rivera vargas j. Leuk Res. 2017 Aug;59:117-123. doi: 10.1016/j.leukres.2017.05.022. Epub 2017 Jun 1. Leuk Res. 2017. PMID: 28624713