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Clinical delineation of a patient with trisomy 1q32.qter and monosomy 5p resulting from a familial translocation 1;5.
Flores Ramírez F, Abreu González M, García Delgado C, Aparicio Onofre A, Guevara Yáñez R, Sánchez Urbina R, Murguía Peniche T, Ramírez-Ortíz MA, Ibarra Ríos D, Ortiz de Luna RI, Cervantes Peredo AB, Morán Barroso VF. Flores Ramírez F, et al. Among authors: guevara yanez r. Genet Couns. 2010;21(4):363-73. Genet Couns. 2010. PMID: 21290965
Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome.
Abreu-González M, García-Delgado C, Cervantes A, Aparicio-Onofre A, Guevara-Yáñez R, Sánchez-Urbina R, Gallegos-Arreola MP, Luna-Angulo A, Estrada FJ, Morán-Barroso VF. Abreu-González M, et al. Among authors: guevara yanez r. Case Rep Genet. 2013;2013:895259. doi: 10.1155/2013/895259. Epub 2013 Sep 18. Case Rep Genet. 2013. PMID: 24151567 Free PMC article.
Cytogenetic studies in children with Down syndrome and acute leukemia.
Valladares A, Palma-Padilla V, Mejía-Aranguré JM, Guevara-Yánez R, Lerma-Reyes A, Salamanca-Gómez F. Valladares A, et al. Among authors: guevara yanez r. Leuk Res. 2005 Nov;29(11):1241-6. doi: 10.1016/j.leukres.2005.03.015. Epub 2005 Apr 25. Leuk Res. 2005. PMID: 16164980
A homozygous CEP57 c.915_925dupCAATGTTCAGC mutation in a patient with mosaic variegated aneuploidy syndrome with rhizomelic shortening in the upper and lower limbs and a narrow thorax.
De la Torre-García O, Mar-Aldama R, Salgado-Sangri R, Diaz-Gomez N, Bonilla-Arcaute L, Diaz-Ponce-Medrano J, Guevara-Yañez R, Córdova EJ, Monge-Cazares T, Orozco L, Martínez-Hernández A. De la Torre-García O, et al. Among authors: guevara yanez r. Eur J Med Genet. 2019 Mar;62(3):195-197. doi: 10.1016/j.ejmg.2018.07.013. Epub 2018 Jul 17. Eur J Med Genet. 2019. PMID: 30010053