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Archives of Medical Research|January 1, 1993
Analysis of dystrophin gene deletions in patients from the Mexican population with Duchenne/Becker muscular dystrophyR Coral-Vázquez, D Arenas, B Cisneros, et al.Archives of Medical Research|January 1, 1996
Molecular diagnosis of Huntington's disease in Mexican patients by polymerase chain reactionB Cisneros Vega, M E Alonso Vilatela, P Yescas Gomez, et al.Molecular Biology Reports|July 17, 2010
Distribution of CTG repeats at the DMPK gene in myotonic dystrophy patients and healthy individuals from the Mexican populationJ J Magaña, P Cortés-Reynosa, R Escobar-Cedillo, et al.American Journal of Medical Genetics|June 13, 1997
Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: the use of new designed primers for the analysis of the major deletion "hot spot" regionR Coral-Vazquez, D Arenas, B Cisneros, et al.FEBS Letters|October 12, 2000
Alternative splicing regulates the nuclear or cytoplasmic localization of dystrophin Dp71E González, C Montañez, P N Ray, et al.Neuroreport|July 7, 1997
Dystrophins in developing retina: Dp260 expression correlates with synaptic maturationF Rodius, T Claudepierre, H Rosas-Vargas, et al.Molecular Biology Reports|October 14, 2014
Altered nuclear structure in myotonic dystrophy type 1-derived fibroblastsR Rodríguez, O Hernández-Hernández, J J Magaña, et al.Archives of Medical Research|January 1, 1993
Carrier detection of hemophilia A in a Mexican population by two Bcl I polymorphismsM D Carrillo Pérez, R Fragoso Herrera, B Cisneros Vega, et al.Archives of Medical Research|January 1, 1996
Carrier detection in Duchenne and Becker muscular dystrophy using dinucleotide repeat polymorphisms. A study in Mexican familiesD Arenas, R Coral, B Cisneros, et al.Clinical Genetics|October 10, 2006
Association of the CT gene (CA) polymorphism with BMD in osteoporotic Mexican womenJ J Magaña, R Gómez, B Cisneros, et al.Pageof 4