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Revista De Neurologia|November 26, 2002
[Experimental therapeutic models for fragile X syndrome]Y de Diego-OteroThe Journal of Laboratory and Clinical Medicine|March 6, 1998
Assessment of FMR1 expression by reverse transcriptase-polymerase chain reaction of KH domainsA Hmadcha, Y De Diego, E PintadoJournal of Medical Genetics|August 3, 2000
Twin sisters, monozygotic with the fragile X mutation, but with a different phenotypeR Willemsen, R Olmer, Y De Diego Otero, et al.Journal of Medical Genetics|November 1, 1995
Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigreeE Pintado, Y de Diego, A Hmadcha, et al.Human Genetics|May 8, 2000
A fragile X case with an amplification/deletion mosaic patternD García Arocena, Y de Diego, B A Oostra, et al.Experimental Cell Research|July 27, 2000
Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouseC E Bakker, Y de Diego Otero, C Bontekoe, et al.Revista De Neurologia|March 1, 2006
[Autosomal recessive diseases with mental retardation]I Fernández-Carvajal, J J Telleria, M Alonso, et al.American Journal of Human Genetics|June 12, 1999
Noninvasive test for fragile X syndrome, using hair root analysisR Willemsen, B Anar, Y De Diego Otero, et al.Revista De Neurologia|March 1, 2005
[Large-scale genotyping in research into autism spectrum disorders and attention deficit hyperactivity disorder]M Bayés, J A Ramos, B Cormand, et al.Revista De Neurologia|March 1, 2006
[Experimental models used in research into genetic disorders that involve intellectual disability]Y de Diego-Otero, Y Romero-Zerbo, R El Bekay, et al.Pageof 2