Unusual clinical phenotype of Stargardt disease
Molina-Solana, Pedro, Morillo-Sánchez, María José, Méndez-Vidal, Cristina, Ramos-Jiménez, Manuel, Domínguez-Serrano, Borja, Antiñolo, Guillermo, Rodríguez-de-la-Rúa-Franch, Enrique
Published in Arquivos brasileiros de oftalmologia (01.07.2021)
Published in Arquivos brasileiros de oftalmologia (01.07.2021)
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Ultrasound, Echocardiography, MRI, and Genetic Analysis of a Fetus with Congenital Diaphragmatic Hernia and Partial 11q Trisomy
Fernández-Perea, Yolanda, García-Díaz, Lutgardo, Sánchez, Javier, Antiñolo, Guillermo, Borrego, Salud
Published in Case reports in obstetrics and gynecology (01.01.2017)
Published in Case reports in obstetrics and gynecology (01.01.2017)
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Association of X-linked hydrocephalus and Hirschsprung disease: Report of a new patient with a mutation in the L1CAM gene
Fernández, Raquel M., Núñez-Torres, Rocío, García-Díaz, Lutgardo, de Agustín, Juan Carlos, Antiñolo, Guillermo, Borrego, Salud
Published in American Journal of Medical Genetics Part A (01.04.2012)
Published in American Journal of Medical Genetics Part A (01.04.2012)
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