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Chromosomal instability in a patient with ring chromosome 14 syndrome: a case report.
Meza-Espinoza JP, González-García JR, Nieto-Marín N, Patrón-Baro LI, González-Arreola RM, Arámbula-Meraz E, Benítez-Pascual J, De la Herrán-Arita AK, Norzagaray-Valenzuela CD, Valdez-Flores MA, Carrillo-Cázares TA, Picos-Cárdenas VJ. Meza-Espinoza JP, et al. Mol Cytogenet. 2024 Jul 18;17(1):17. doi: 10.1186/s13039-024-00686-0. Mol Cytogenet. 2024. PMID: 39020403 Free PMC article.
Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat.
Meza-Espinoza JP, Sáinz González E, León-León CJN, Arámbula-Meraz E, Contreras-Gutiérrez JA, García-Magallanes N, Madueña-Molina J, Luque-Ortega F, Cervín-Serrano S, Picos-Cárdenas VJ. Meza-Espinoza JP, et al. Mol Cytogenet. 2020 May 19;13:17. doi: 10.1186/s13039-020-00484-4. eCollection 2020. Mol Cytogenet. 2020. PMID: 32467733 Free PMC article.
Cytogenomic characterization of a de novo 4q34.1 deletion in a girl with mild dysmorphic features and a coagulation disorder.
Meza-Espinoza JP, Contreras-Gutiérrez JA, Arámbula-Meraz E, González-García JR, Domínguez-Quezada MG, García-Magallanes N, Madueña-Molina J, Benítez-Pascual J, Partida-Pérez M, Picos-Cárdenas VJ. Meza-Espinoza JP, et al. Mol Cytogenet. 2021 Sep 4;14(1):43. doi: 10.1186/s13039-021-00564-z. Mol Cytogenet. 2021. PMID: 34481514 Free PMC article.
Novel TINF2 gene mutation in dyskeratosis congenita with extremely short telomeres: A case report.
Picos-Cárdenas VJ, Beltrán-Ontiveros SA, Cruz-Ramos JA, Contreras-Gutiérrez JA, Arámbula-Meraz E, Angulo-Rojo C, Guadrón-Llanos AM, Leal-León EA, Cedano-Prieto DM, Meza-Espinoza JP. Picos-Cárdenas VJ, et al. Among authors: meza espinoza jp. World J Clin Cases. 2022 Nov 26;10(33):12440-12446. doi: 10.12998/wjcc.v10.i33.12440. World J Clin Cases. 2022. PMID: 36483815 Free PMC article.
31 results