Search Results - "Verson, C. Alaez"

Identification through exome sequencing of the first PMM2-CDG individual of Mexican mestizo origin by González-Domínguez, C.A., Raya-Trigueros, A., Manrique-Hernández, S., González Jaimes, A., Salinas-Marín, R., Molina-Garay, C., Carrillo-Sánchez, K., Flores-Lagunes, L.L., Jiménez-Olivares, M., Dehesa-Caballero, C., Alaez-Versón, C., Martínez-Duncker, I.

“…Congenital Disorders of Glycosylation (CDG) are scarcely reported from Latin America. We here report on a Mexican mestizo with a multi-systemic syndrome…”
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Prevalence of DNA-Repair Gene mutations in Mexican men with prostate cancer by Cruz Garcia Villa, P., Izunza Laisequilla, A., Puga Ortega, E., Alaez Verson, C.

“…Mexico reported 26,742 new cases of prostate cancer in 2020. Different risk factors have been identified in the pathogenesis of prostate cancer. Among them,…”
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Non-functional alternative splicing caused by a Latino pathogenic variant in a case of PMM2-CDG by González-Domínguez, C.A., Villarroel, C.E., Rodríguez-Morales, M., Manrique-Hernández, S., González-Jaimes, A., Olvera-Rodriguez, F., Beutelspacher, K., Molina-Garay, C., Carrillo-Sánchez, K., Flores-Lagunes, L.L., Jiménez-Olivares, M., Muñoz-Rivas, A., Cruz-Muñoz, M.E., Mora-Montes, H.M., Salinas-Marín, R., Alaez-Verson, C., Martínez-Duncker, I.

“…We report on a Mexican mestizo with a multisystemic syndrome including neurological involvement and a type I serum transferrin isoelectric focusing (Tf IEF)…”
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Topic: AS01-Diagnosis/AS01c-Molecular aberrations (cytogenetic, genetic, gene expression): REAL-WORLD LABORATORY PRACTICE PATTERNS ON NEXT-GENERATION-SEQUENCING (NGS) TECHNOLOGY IN LATIN AMERICA by Belli, C., Bender, A., Jauk, F., Alonso, C., Asinari, M., Rahhal, M., De Paula Sabino, A., Duarte, F., Calado, R., Campregher, P., Yunis, J., Urrea, C. Cortes, Fortuny, M. Villegas, Verson, C. Alaez, De Leon, A. Gomez, Lugo, A. Ayala, Olmedo, Y., Guerra, P. Ortiz, García, P., Valladares, X., Grille, S.

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Non-functional alternative splicing caused by a Latino pathogenic variant in a case of PMM2-CDG by González-Domínguez, C A, Villarroel, C E, Rodríguez-Morales, M, Manrique-Hernández, S, González-Jaimes, A, Olvera-Rodriguez, F, Beutelspacher, K, Molina-Garay, C, Carrillo-Sánchez, K, Flores-Lagunes, L L, Jiménez-Olivares, M, Muñoz-Rivas, A, Cruz-Muñoz, M E, Mora-Montes, H M, Salinas-Marín, R, Alaez-Verson, C, Martínez-Duncker, I

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Rearrangement of the alpha RAR and pml genes in promyelocytic leukemia by Corral Abascal, L, Muñiz Fernández, A, Alaez Verson, C, Hernández Pérez, G, Espinosa Martínez, E, González Otero, A, Hernández Ramírez, P, Martínez Antuña, G

“…The purpose of this work was to assess the re-arrangement of RAR-alpha and pml genes in a group of patients with acute promyelocytic leukaemia (APL) in…”
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Identification through exome sequencing of the first PMM2-CDG individual of Mexican mestizo origin by González-Domínguez, C A, Raya-Trigueros, A, Manrique-Hernández, S, González Jaimes, A, Salinas-Marín, R, Molina-Garay, C, Carrillo-Sánchez, K, Flores-Lagunes, L L, Jiménez-Olivares, M, Dehesa-Caballero, C, Alaez-Versón, C, Martínez-Duncker, I

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