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A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient.
Genet Couns. 2010;21(3):299-306.
Genet Couns. 2010.
PMID: 20964121
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
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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.
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Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q.
Martín-De Saro MD, Valdés-Miranda JM, Plaza-Benhumea L, Pérez-Cabrera A, Gonzalez-Huerta LM, Guevara-Yañez R, Cuevas-Covarrubias SA.
Martín-De Saro MD, et al. Among authors: guevara yanez r.
Cytogenet Genome Res. 2015;147(2-3):124-9. doi: 10.1159/000444138. Epub 2016 Feb 23.
Cytogenet Genome Res. 2015.
PMID: 26900692
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PCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype.
Cervantes A, Guevara-Yáñez R, López M, Monroy N, Aguinaga M, Valdez H, Sierra C, Canún S, Guízar J, Navarrete C, Zafra G, Salamanca F, Kofman-Alfaro S.
Cervantes A, et al. Among authors: guevara yanez r.
Clin Genet. 2001 Nov;60(5):385-92. doi: 10.1034/j.1399-0004.2001.600512.x.
Clin Genet. 2001.
PMID: 11903342
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A girl with 15q overgrowth syndrome and dup(15)(q24q26.3) that included telomeric sequences.
Gutiérrez-Franco Mde L, Madariaga-Campos Mde L, Vásquez-Velásquez AI, Matute E, Guevara-Yáñez R, Rivera H.
Gutiérrez-Franco Mde L, et al. Among authors: guevara yanez r.
Korean J Lab Med. 2010 Jun;30(3):318-24. doi: 10.3343/kjlm.2010.30.3.318.
Korean J Lab Med. 2010.
PMID: 20603595
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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
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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
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