Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis
Córdova-Fletes, Carlos, Rangel-Sosa, Martha M., Martínez-Jacobo, Lizeth A., Becerra-Solano, Luis Eduardo, Arellano-Valdés, Carmen Araceli, Tlacuilo-Parra, José Alberto, Galán-Huerta, Kame Alberto, Rivas-Estilla, Ana María, Hernandez-Orozco, Angélica Alejandra, García-Ortiz, José Elías
Published in Autoimmunity (Chur, Switzerland) (17.08.2020)
Published in Autoimmunity (Chur, Switzerland) (17.08.2020)
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Microcephaly, an etiopathogenic vision
Becerra-Solano, Luis Eduardo, Mateos-Sánchez, Leovigildo, López-Muñoz, Eunice
Published in Pediatrics and neonatology (01.07.2021)
Published in Pediatrics and neonatology (01.07.2021)
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Severe Craniofacial Involvement due to Amniotic Band Sequence
Becerra-Solano, Luis Eduardo, Castañeda-Cisneros, Gema, Corona-Rivera, Jorge Roman, Díaz-Rodríguez, Manuel, Figuera, Luis Eduardo, López-Muñoz, Eunice, Nastasi-Catanese, José Antonio, Toscano-Flores, José Jesús, Ramírez-Dueñas, María de Lourdes, García-Ortíz, José Elias
Published in Fetal and pediatric pathology (02.01.2018)
Published in Fetal and pediatric pathology (02.01.2018)
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Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis
Herrera-Tirado, Isis Mariela, Espinoza-Mata, Laura Lucia, Rizo-delaTorre, Lourdes Del Carmen, Becerra-Solano, Luis Eduardo, Ibarra-Cortés, Bertha, Perea-Díaz, Francisco Javier
Published in Genetic testing and molecular biomarkers (01.05.2022)
Published in Genetic testing and molecular biomarkers (01.05.2022)
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Journal Article
Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Tyr370Cys) in NEU1
Flores-Contreras, Elda Ariadna, García-Ortiz, José Elías, Robles-Espinoza, Carla Daniela, Zomosa-Signoret, Viviana, Becerra-Solano, Luis Eduardo, Vidaltamayo, Román, Castaneda-García, Carolina, Esparza-García, Eduardo, Molina-Aguilar, Christian, Hernández-Orozco, Angélica Alejandra, Córdova-Fletes, Carlos
Published in Molecular syndromology (01.07.2021)
Published in Molecular syndromology (01.07.2021)
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Journal Article
Causas del hidrops fetal: experiencia en un hospital obstétrico del Occidente de México
Becerra-Solano, Luis Eduardo, Medina-Castellanos, Marcela, Oseguera-Torres, Luis Fernando, Mendoza-Ruvalcaba, Sandra del Carmen, Domínguez-Quezada, María Guadalupe, García-Ortiz, José Elías
Published in Ginecologia y obstetricia de Mexico (01.07.2022)
Published in Ginecologia y obstetricia de Mexico (01.07.2022)
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Journal Article
Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Tyr370Cys) in NEU1
Flores-Contreras, Elda Ariadna, García-Ortiz, José Elías, Robles-Espinoza, Carla Daniela, Zomosa-Signoret, Viviana, Becerra-Solano, Luis Eduardo, Vidaltamayo, Román, Castaneda-García, Carolina, Esparza-García, Eduardo, Molina-Aguilar, Christian, Hernández-Orozco, Angélica Alejandra, Córdova-Fletes, Carlos
Published in Molecular syndromology (01.07.2021)
Published in Molecular syndromology (01.07.2021)
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