Familial exudative vitreoretinopathy: A report of an asymptomatic case with autosomal dominant inheritance detected using FZD4 molecular analysis

Autor: Montecinos-Contreras, C., Sepúlveda-Vázquez, H.E., Pelcastre-Luna, E., Zenteno, J.C., Villanueva-Mendoza, C.

Publikováno v: In Archivos de la Sociedad Española de Oftalmología (English Ed) April 2017 92(4):189-192

Vitreorretinopatía exudativa familiar, reporte de un caso asintomático con herencia autosómica dominante, detectado mediante análisis molecular de FZD4

Autor: Montecinos-Contreras, C., Sepúlveda-Vázquez, H.E., Pelcastre-Luna, E., Zenteno, J.C., Villanueva-Mendoza, C.

Publikováno v: Archivos de la Sociedad Española de Oftalmología; April 2017, Vol. 92 Issue: 4 p189-192, 4p

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Identification and expression analysis of a novel intragenic EFNB1 mutation causing craniofrontonasal syndrome.

Autor: Chacon-Camacho OF; Department of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico., Arce-Gonzalez R; Department of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico., Villegas-Ruiz V; Department of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico., Pelcastre-Luna E; Department of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico., Uría-Gómez CE; Laboratorio de Genética, Facultad de Medicina, UAEM, Toluca, State of Mexico, Mexico., Granillo-Alvarez M; Department of Obstetrics and Gynaecology, HGZ No. 76, Instituto Mexicano del Seguro Social, State of Mexico, Mexico., Zenteno JC; Department of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico ; Department of Biochemistry, Faculty of Medicine, National Autonomous University of Mexico (UNAM), Mexico City, Mexico.

Publikováno v: Meta gene [Meta Gene] 2013 Nov 28; Vol. 2, pp. 25-31. Date of Electronic Publication: 2013 Nov 28 (Print Publication: 2014).