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Boletin Medico Del Hospital Infantil De Mexico|September 13, 2022
Congenital hearing loss: a literature review of the genetic etiology in a Mexican populationCarlos de la Torre-González, Dina Villanueva-García, Constanza García-Delgado, et al.Annals of Hepatology|May 25, 2019
Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican populationMagdalena Cerón-Rodríguez, Edgar Ricardo Vázquez-Martínez, Constanza García-Delgado, et al.Meta Gene|January 22, 2015
Polymorphism analysis and new JAG1 gene mutations of Alagille syndrome in Mexican populationEdgar Ricardo Vázquez-Martínez, Gustavo Varela-Fascinetto, Constanza García-Delgado, et al.Ophthalmic Genetics|September 19, 2017
Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literatureLaura Gómez-Laguna, Alejandro Martínez-Herrera, Alejandra Del Pilar Reyes-de la Rosa, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 28, 2014
Brachmann-Cornelia de Lange syndrome with a papilloma of the choroid plexus: analyses of molecular genetic characteristics of the patient and the tumor. A single-case studyFernando Chico-Ponce de León, Luis F Gordillo-Domínguez, Vicente González-Carranza, et al.International Journal of Pediatric Otorhinolaryngology|September 28, 2015
Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart diseaseCandy Sue Márquez-Ávila, Alfredo Vizcaíno-Alarcón, Constanza García-Delgado, et al.Pageof 2