Hasil Pencarian - Víctor Martínez-Glez

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  1. 1
    Biomarkers in Vestibular Schwannoma–Associated Hearing Loss

    Biomarkers in Vestibular Schwannoma–Associated Hearing Loss oleh Luis Lassaletta, Luis Lassaletta, Luis Lassaletta, Miryam Calvino, Miryam Calvino, Jose Manuel Morales-Puebla, Pablo Lapunzina, Pablo Lapunzina, Pablo Lapunzina, Lourdes Rodriguez-de la Rosa, Lourdes Rodriguez-de la Rosa, Lourdes Rodriguez-de la Rosa, Isabel Varela-Nieto, Isabel Varela-Nieto, Isabel Varela-Nieto, Victor Martinez-Glez, Victor Martinez-Glez, Victor Martinez-Glez

    Diterbitkan 2019-09-01
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  2. 2
    Sirolimus Early Treatment in Vascular Anomalies Leads to a Better Response

    Sirolimus Early Treatment in Vascular Anomalies Leads to a Better Response oleh Paloma Triana, Jesús Díez-Sebastián, Lara Rodriguez-Laguna, Victor Martinez-Glez, Juan Carlos Lopez-Gutierrez

    Diterbitkan 2023-03-01
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  3. 3
    Impact of NGS in the medical sciences: genetic syndromes with an increased risk of developing cancer as an example of the use of new technologies

    Impact of NGS in the medical sciences: genetic syndromes with an increased risk of developing cancer as an example of the use of new technologies oleh Pablo Lapunzina, Rocío Ortiz López, Lara Rodríguez-Laguna, Purificación García-Miguel, Augusto Rojas Martínez, Víctor Martínez-Glez

    Diterbitkan 2014-01-01
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  4. 4
    Case report: Identification of a novel variant p.Gly215Arg in the CHN1 gene causing Moebius syndrome

    Case report: Identification of a novel variant p.Gly215Arg in the CHN1 gene causing Moebius syndrome oleh Carmen Manso-Bazús, Nino Spataro, Elisabeth Gabau, Viviana P. Beltrán-Salazar, Juan Pablo Trujillo-Quintero, Nuria Capdevila, Anna Brunet-Vega, Neus Baena, A Arockia Jeyaprakash, A Arockia Jeyaprakash, Victor Martinez-Glez, Anna Ruiz

    Diterbitkan 2024-01-01
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  5. 5
    New microdeletion and microduplication syndromes: a comprehensive review

    New microdeletion and microduplication syndromes: a comprehensive review oleh Julián Nevado, Rafaella Mergener, María Palomares-Bralo, Karen Regina Souza, Elena Vallespín, Rocío Mena, Víctor Martínez-Glez, María Ángeles Mori, Fernando Santos, Sixto García-Miñaur, Fé García-Santiago, Elena Mansilla, Luis Fernández, María Luisa de Torres, Mariluce Riegel, Pablo Lapunzina

    Diterbitkan 2014-01-01
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  6. 6
    Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor.

    Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor. oleh Leila Cabral de Almeida Cardoso, Lara Rodriguez-Laguna, María Del Carmen Crespo, Elena Vallespín, María Palomares-Bralo, Rubén Martin-Arenas, Inmaculada Rueda-Arenas, Paulo Antonio Silvestre de Faria, GT-CSGP Working Group, Purificación García-Miguel, Pablo Lapunzina, Fernando Regla Vargas, Hector N Seuanez, Víctor Martínez-Glez

    Diterbitkan 2015-01-01
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  7. 7
    Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy

    Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy oleh María Cristina Estañ, Elisa Fernández-Núñez, Maha S. Zaki, María Isabel Esteban, Sandra Donkervoort, Cynthia Hawkins, José A. Caparros-Martin, Dimah Saade, Ying Hu, Véronique Bolduc, Katherine Ru-Yui Chao, Julián Nevado, Ana Lamuedra, Raquel Largo, Gabriel Herrero-Beaumont, Javier Regadera, Concepción Hernandez-Chico, Eduardo F. Tizzano, Victor Martinez-Glez, Jaime J. Carvajal, Ruiting Zong, David L. Nelson, Ghada A. Otaify, Samia Temtamy, Mona Aglan, Mahmoud Issa, Carsten G. Bönnemann, Pablo Lapunzina, Grace Yoon, Victor L. Ruiz-Perez

    Diterbitkan 2019-02-01
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