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Pediatrics and Neonatology|June 11, 2021
Microcephaly, an etiopathogenic visionLuis Eduardo Becerra-Solano, Leovigildo Mateos-Sánchez, Eunice López-Muñoz
Journal of Applied Genetics|February 3, 2007
A 9p13-->p24 duplication coupled with a whole 22q translocation onto 9p24Horacio Rivera, Ana I Vásquez-Velásquez, Mariá de Lourdes Ramirez-Duenas, et al.
Genetic Testing and Molecular Biomarkers|May 31, 2022
Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary SpherocytosisIsis Mariela Herrera-Tirado, Laura Lucia Espinoza-Mata, Lourdes Del Carmen Rizo-delaTorre, et al.
Nutricion Hospitalaria|January 8, 2026
Association of IL-18 gene variants with depressive symptoms and metabolic syndrome in Mexican adultsMonica Lizeth Ramirez De Los Santos, Saúl Ramírez-De Los Santos, Luis Eduardo Becerra Solano, et al.
Molecular Syndromology|August 23, 2021
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 NEU1Elda Ariadna Flores-Contreras, José Elías García-Ortiz, Carla Daniela Robles-Espinoza, et al.
Fetal and Pediatric Pathology|January 17, 2018
Severe Craniofacial Involvement due to Amniotic Band SequenceLuis Eduardo Becerra-Solano, Gema Castañeda-Cisneros, Jorge Roman Corona-Rivera, et al.
Autoimmunity|June 30, 2020
Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositisCarlos Córdova-Fletes, Martha M Rangel-Sosa, Lizeth A Martínez-Jacobo, et al.
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