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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.
Case Rep Genet. 2013;2013:895259. doi: 10.1155/2013/895259. Epub 2013 Sep 18.
Case Rep Genet. 2013.
PMID: 24151567
Free PMC article.
A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient.
García-Delgado C, Bahena-Martínez E, Aparicio-Onofre A, Guevara-Yañez R, Cervantes-Peredo A, Azotla-Vilchis OC, Estrada-Mena J, Luna-Angulo A, Villa-Morales J, Moran-Barroso VF.
García-Delgado C, et al. Among authors: aparicio onofre a.
Genet Couns. 2010;21(3):299-306.
Genet Couns. 2010.
PMID: 20964121
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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: aparicio onofre a.
Genet Couns. 2010;21(4):363-73.
Genet Couns. 2010.
PMID: 21290965
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