Showing 1 - 6 results of 6 for search 'Milagros Balbín', query time: 0.03s Refine Results
  1. 1
    El diagnóstico molecular en la praxis de la oncología en el Sector Salud. El laboratorio de oncología molecular como herramienta

    El diagnóstico molecular en la praxis de la oncología en el Sector Salud. El laboratorio de oncología molecular como herramienta by Víctor Manuel Valdespino-Gómez, Milagros Balbín-Felechosa

    Published 2016-12-01
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  2. 2
    Relevance of Germline Mutation Screening in Both Familial and Sporadic Head and Neck Paraganglioma for Early Diagnosis and Clinical Management

    Relevance of Germline Mutation Screening in Both Familial and Sporadic Head and Neck Paraganglioma for Early Diagnosis and Clinical Management by Mario A. Hermsen, María A. Sevilla, José Luis Llorente, Marjan M. Weiss, Anneliese Grimbergen, Eva Allonca, Cristina Garcia-Inclán, Milagros Balbín, Carlos Suárez

    Published 2010-01-01
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  3. 3
    Fatal sclerosing mesenteritis: a 7-year-old male autopsy case report

    Fatal sclerosing mesenteritis: a 7-year-old male autopsy case report by Juan Carlos Celis Pinto, Lucía Hernández Peláez, Guillermo Mendoza Pacas, Juan Mayordomo Colunga, Milagros Balbín, Ana Pitiot, Héctor-Enrique Torres-Rivas, Verónica Blanco Lorenzo

    Published 2023-05-01
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  4. 4
    A t(1;9) translocation involving CSF3R as a novel mechanism in unclassifiable chronic myeloproliferative neoplasm

    A t(1;9) translocation involving CSF3R as a novel mechanism in unclassifiable chronic myeloproliferative neoplasm by Jesús Gutiérrez-Abril, Iñigo Santamaría, Ana S. Pitiot, Ana Gutiérrez-Fernández, Ángel Alvarez-Eguiluz, José M. Vicente, Carmen Sanzo, Soledad González-Muñiz, Milagros Balbín, Xose S. Puente

    Published 2017-12-01
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  5. 5
    PanCancer analysis of somatic mutations in repetitive regions reveals recurrent mutations in snRNA U2

    PanCancer analysis of somatic mutations in repetitive regions reveals recurrent mutations in snRNA U2 by Pablo Bousquets-Muñoz, Ander Díaz-Navarro, Ferran Nadeu, Ana Sánchez-Pitiot, Sara López-Tamargo, Shimin Shuai, Milagros Balbín, Jose M. C. Tubio, Sílvia Beà, Jose I. Martin-Subero, Ana Gutiérrez-Fernández, Lincoln D. Stein, Elías Campo, Xose S. Puente

    Published 2022-03-01
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  6. 6
    Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma

    Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma by Sara Mellid, Eduardo Gil, Rocío Letón, Eduardo Caleiras, Emiliano Honrado, Susan Richter, Nuria Palacios, Marcos Lahera, Juan C. Galofré, Adriá López-Fernández, Maria Calatayud, Aura D. Herrera-Martínez, María A. Galvez, Xavier Matias-Guiu, Milagros Balbín, Esther Korpershoek, Eugénie S. Lim, Francesca Maletta, Sofia Lider, Stephanie M. J. Fliedner, Nicole Bechmann, Graeme Eisenhofer, Graeme Eisenhofer, Letizia Canu, Elena Rapizzi, Irina Bancos, Mercedes Robledo, Mercedes Robledo, Alberto Cascón, Alberto Cascón

    Published 2023-01-01
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