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Issue DateTitleAuthor(s)
Jun-2020Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositisCórdova 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
Jul-2021Microcephaly, an etiopathogenic visionBecerra Solano, Luis Eduardo; Mateos Sanchez, Leovigildo; Lopez Munoz, Eunice
May-2022Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary SpherocytosisHerrera Tirado, Isis Mariela; Espinoza Mata, Laura Lucía; Rizo De la Torre, Lourdes del Carmen; Becerra Solano, Luis Eduardo; Ibarra Cortés, Bertha; Perea Díaz, Francisco Javier
Jul-2021Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum DisorderGarcía Ortiz, José Elías; Zarazúa Niño, Ana Itzel; Hernández Orozco, Angélica Alejandra; Reyes Oliva, Edwin A; Pérez Ávila, Carlos E.; Becerra Solano, Luis Eduardo; Galán Huerta, Kame A; Rivas Estilla, Ana María; Córdova Fletes, Carlos
Jul-2022Causas del hidrops fetal: experiencia en un hospital obstétrico del Occidente de MéxicoBecerra Solano, Luis Eduardo; Medina Castellanos, Marcela; Oseguera Torres, Luis Fernando; Mendoza Ruvalcaba, Sandra del Carmen; Domínguez Quezada, María Guadalupe; García Ortiz, José Elías