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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.
Promoter polymorphism of the serotonin transporter gene influences the number of sexual partners and smoking habits in a Mexican Mestizo population.
Peralta-Leal V, Leal-Ugarte E, Gutiérrez-Angulo M, Dávalos-Rodríguez IP, Gallegos-Arreola MP, Meza-Espinoza JP, Torres-Benavides HG, Peregrina-Sandoval J, Villarreal-Sotelo K, Ondarza Rodríguez MM, Nair S, Durán-González J. Peralta-Leal V, et al. Psychiatr Genet. 2015 Aug;25(4):178-9. doi: 10.1097/YPG.0000000000000089. Psychiatr Genet. 2015. PMID: 25919451 No abstract available.
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.
29 results