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High occurrence of CRLF2 abnormalities in Mexican children with B-cell acute lymphoblastic leukemia.
Juárez-Velázquez MDR, Moreno-Lorenzana DL, Martínez Anaya DA, Hernández Monterde EA, Aguilar-Hernández MM, Reyes-León A, Chávez-González MA, López Santiago N, Zapata Tarrés M, Juárez Villegas L, Rivera Sánchez N, Soto Lerma O, Vega-Vega L, Rivera Luna R, Pérez-Vera P. Juárez-Velázquez MDR, et al. Among authors: martinez anaya da. Cytokine. 2022 Jul;155:155896. doi: 10.1016/j.cyto.2022.155896. Epub 2022 May 7. Cytokine. 2022. PMID: 35537330
CRLF2 and IKZF1 abnormalities in Mexican children with acute lymphoblastic leukemia and recurrent gene fusions: exploring surrogate markers of signaling pathways.
Moreno Lorenzana D, Juárez Velázquez MDR, Reyes León A, Martínez Anaya D, Hernández Monterde A, Salas Labadía C, Navarrete Meneses MDP, Zapata Tarrés M, Juárez Villegas L, Jarquín Ramírez B, Cárdenas Cardós R, Herrera Almanza M, Paredes Aguilera R, Pérez Vera P. Moreno Lorenzana D, et al. J Pathol Clin Res. 2021 Jul;7(4):410-421. doi: 10.1002/cjp2.211. Epub 2021 Apr 23. J Pathol Clin Res. 2021. PMID: 33890726 Free PMC article.
Characterization of Philadelphia-like Pre-B Acute Lymphoblastic Leukemia: Experiences in Mexican Pediatric Patients.
Martínez-Anaya D, Moreno-Lorenzana D, Reyes-León A, Juárez-Figueroa U, Dean M, Aguilar-Hernández MM, Rivera-Sánchez N, García-Islas J, Vieyra-Fuentes V, Zapata-Tarrés M, Juárez-Villegas L, Paredes-Aguilera R, Vega-Vega L, Rivera-Luna R, Juárez-Velázquez MDR, Pérez-Vera P. Martínez-Anaya D, et al. Int J Mol Sci. 2022 Aug 24;23(17):9587. doi: 10.3390/ijms23179587. Int J Mol Sci. 2022. PMID: 36076986 Free PMC article.
The relevance of the cytogenetic analysis in syndromic microphthalmia/anophthalmia.
Apam-Garduño D, Cortés-González V, Quintana-Fernández L, Martínez-Anaya D, Pérez-Vera P, Villanueva-Mendoza C. Apam-Garduño D, et al. Ophthalmic Genet. 2019 Dec;40(6):584-587. doi: 10.1080/13816810.2019.1698618. Epub 2019 Dec 6. Ophthalmic Genet. 2019. PMID: 31809626 No abstract available.
Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations.
Salas-Labadía C, Gómez-Carmona S, Cruz-Alcívar R, Martínez-Anaya D, Del Castillo-Ruiz V, Durán-McKinster C, Ulloa-Avilés V, Yokoyama-Rebollar E, Ruiz-Herrera A, Navarrete-Meneses P, Lieberman-Hernández E, González-Del Angel A, Cervantes-Barragán D, Villarroel-Cortés C, Reyes-León A, Suárez-Pérez D, Pedraza-Meléndez A, González-Orsuna A, Pérez-Vera P. Salas-Labadía C, et al. Orphanet J Rare Dis. 2019 Nov 15;14(1):259. doi: 10.1186/s13023-019-1208-0. Orphanet J Rare Dis. 2019. PMID: 31730496 Free PMC article.