Hasil Pencarian - Emiy Yokoyama

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  1. 1
    Abordaje citogenético y citogenómico de pacientes con discapacidad intelectual y malformaciones congénitas

    Abordaje citogenético y citogenómico de pacientes con discapacidad intelectual y malformaciones congénitas oleh Emiy Yokoyama-Rebollar, Sara Frías, Victoria del Castillo-Ruiz

    Diterbitkan 2017-11-01
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  2. 2
    Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review

    Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review oleh Emiy Yokoyama, Camilo E. Villarroel, Sinhué Diaz, Victoria Del Castillo, Patricia Pérez-Vera, Consuelo Salas, Samuel Gómez, Reneé Barreda, Bertha Molina, Sara Frias

    Diterbitkan 2020-09-01
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  3. 3
    7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype

    7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype oleh Emiy Yokoyama, Dennise Lesley Smith-Pellegrin, Silvia Sánchez, Bertha Molina, Alfredo Rodríguez, Rocío Juárez, Esther Lieberman, Silvia Avila, José Luis Castrillo, Victoria del Castillo, Sara Frías

    Diterbitkan 2017-11-01
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  4. 4
    Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics

    Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics oleh Emiy Yokoyama, Victoria Del Castillo, Silvia Sánchez, Sandra Ramos, Bertha Molina, Leda Torres, María José Navarro, Silvia Avila, José Luis Castrillo, Benilde García-De Teresa, Bárbara Asch, Sara Frías

    Diterbitkan 2018-05-01
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  5. 5
    Frequent copy number variants in a cohort of Mexican-Mestizo individuals

    Frequent copy number variants in a cohort of Mexican-Mestizo individuals oleh Silvia Sánchez, Ulises Juárez, Julieta Domínguez, Bertha Molina, Rehotbevely Barrientos, Angélica Martínez-Hernández, Alessandra Carnevale, Patricia Grether-González, Dora Gilda Mayen, Camilo Villarroel, Esther Lieberman, Emiy Yokoyama, Victoria Del Castillo, Leda Torres, Sara Frias

    Diterbitkan 2023-01-01
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  6. 6
    Cryptorchidism and Testicular Tumor: Comprehensive Analysis of Common Clinical Features and Search of SNVs in the KIT and AR Genes

    Cryptorchidism and Testicular Tumor: Comprehensive Analysis of Common Clinical Features and Search of SNVs in the KIT and AR Genes oleh Daniel Adrian Landero-Huerta, Daniel Adrian Landero-Huerta, Rosa María Vigueras-Villaseñor, Emiy Yokoyama-Rebollar, Fabiola García-Andrade, Julio César Rojas-Castañeda, Luis Alonso Herrera-Montalvo, Luis Alonso Herrera-Montalvo, José Díaz-Chávez, Isidro Xavier Pérez-Añorve, Elena Aréchaga-Ocampo, Margarita Dolores Chávez-Saldaña

    Diterbitkan 2020-08-01
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  7. 7
    Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico

    Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico oleh Paula Leal-Anaya, Paula Leal-Anaya, Paula Leal-Anaya, Tamara N. Kimball, Ana Lucia Yanez-Felix, Moisés Ó. Fiesco-Roa, Moisés Ó. Fiesco-Roa, Benilde García-de Teresa, Benilde García-de Teresa, Angélica Monsiváis, Rocío Juárez-Velázquez, Esther Lieberman, Camilo Villarroel, Emiy Yokoyama, Liliana Fernández-Hernández, Anet Rivera-Osorio, David Sosa, Maria Magdalena Ortiz Sandoval, Norma López-Santiago, Sara Frías, Sara Frías, Victoria del Castillo, Alfredo Rodríguez, Alfredo Rodríguez

    Diterbitkan 2024-01-01
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