Estudio multidisciplinario del paciente con anemia de Fanconi by Benilde García de Teresa, Alfredo Rodríguez, Sara Frías

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Mitosis and its regulation by Alfredo de Jesús Rodríguez-Gómez, Sara Frías-Vázquez

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Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences by Benilde García-de-Teresa, Alfredo Rodríguez, Sara Frias

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

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Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5 days post-coitum in ear and back skin tissues by Leda Torres, Ulises Juárez, Laura García, Juan Miranda-Ríos, Sara Frias

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Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability by Moisés Ó. Fiesco-Roa, Moisés Ó. Fiesco-Roa, Benilde García-de Teresa, Paula Leal-Anaya, Renée van ‘t Hek, Talia Wegman-Ostrosky, Sara Frías, Sara Frías, Alfredo Rodríguez, Alfredo Rodríguez

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Translocaciones crípticas de cromosomas acrocéntricos en muestras de tejido de aborto aneuploide by Sandra Ramos, Bertha Molina, Patricia Grether, Dora Gilda Mayén, Oscar Castro, Marta Ángeles, Rebeca Rodríguez, Sara Frías

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Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells by Rosalba Sevilla-Montoya, Maria de Jesus Zavaleta-Abreu, Gloria Queipo, Silvia Sanchez, Sara Frias, Alberto Hidalgo-Bravo, Patricia Grether-González

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

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FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México by Benilde García‐de Teresa, Sara Frias, Bertha Molina, María Teresa Villarreal, Alfredo Rodriguez, Alessandra Carnevale, Gerardo López‐Hernández, Lilia Vollbrechtshausen, Alberto Olaya‐Vargas, Leda Torres

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7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype by 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

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P659: A comprehensive genotyping study in Mexican patients with Fanconi anemia identified reported, novel, and founder pathogenic variants by Leda Torres, Pedro Reyes, Benilde García-de Teresa, María Teresa Villarreal Molina, Ulises Juárez, Angélica Solis, Moises Fiesco-Roa, Fernando Pérez Villatoro, Bertha Molina, Alfredo Rodríguez, Alessandra Carnevale, Sara Frías

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Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in <i>FANCG</i> by Pedro Reyes, Benilde García-de Teresa, Ulises Juárez, Fernando Pérez-Villatoro, Moisés O. Fiesco-Roa, Alfredo Rodríguez, Bertha Molina, María Teresa Villarreal-Molina, Jorge Meléndez-Zajgla, Alessandra Carnevale, Leda Torres, Sara Frias

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Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico by 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

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Estudio cromosómico de 303 pérdidas gestacionales en México by Luz M. Garduño-Zarazúa, Dora G. Mayén, Ricardo Meléndez-Hernández, Antonio J. Paz-Martínez, Eva Ramírez-Arroyo, David Sosa, Mónica Aguinaga, Javier Pérez-Durán, Osiris Ríos, Jaime López-Valdez, Leda Torres, Sara Frías

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Frequent copy number variants in a cohort of Mexican-Mestizo individuals by 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

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TGFβ pathway is required for viable gestation of Fanconi anemia embryos. by Alfredo Rodríguez, Michael Epperly, Jessica Filiatrault, Martha Velázquez, Chunyu Yang, Kelsey McQueen, Larissa A Sambel, Huy Nguyen, Divya Ramalingam Iyer, Ulises Juárez, Cecilia Ayala-Zambrano, David B Martignetti, Sara Frías, Renee Fisher, Kalindi Parmar, Joel S Greenberger, Alan D D'Andrea

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P263: Genotype-phenotype associations in CASK disorders: A systematic literature review and report of three cases by Andrea Medina-Huerta, Paulina Gómez-Moreno, Gabriela Baltazar-Escobar, Mariana Berzunza, Anaid Dordelly-Hernández, Abed Ramírez, Jaime López-Valdez, Cristian Muñoz Sánchez, Silvia Sánchez-Sandoval, Miguel Rodríguez-Morales, Pedro Reyes, Leda Torres, Liliae Bustamante-Montes, Sara Frías, Rodrigo Ugalde-Resano, Moises Fiesco-Roa

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P191: Old school and new findings: Expansion and delineation of the dysmorphological phenotype of Fanconi anemia by Moises Fiesco-Roa, Andrea Venegas-Andrade, María del Mar Sáez de Ocariz Gutiérrez, Sonia Toussaint-Caire, Armando Hernández Rodas, Gilberto Gómez Garza, Magdalena Ortiz Sandoval, Elia Ixel Apodaca Chávez, Leda Torres, Pedro Reyes, Ulises Juárez, Angélica Solis, Bertha Molina, Alfredo Rodríguez, Sara Frías, Benilde García-de Teresa

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