Research of Fragile X Syndrome has been linked to Sex Chromosome Aberrations, Autistic Disorder, Trinucleotide Repeat Expansion, Ataxia, Down Syndrome. The study of Fragile X Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Fragile X Syndrome include Methylation, Translation, Pathogenesis, Cognition, Localization. These pathways complement our catalog of research reagents for the study of Fragile X Syndrome including antibodies and ELISA kits against FMR1, RABEP2, FOSL1, NUFIP2, AFF2.
Top Research Reagents
We have 1813 products for the study of Fragile X Syndrome that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Fragile X Syndrome is also known as fragile x syndrome, fraxa syndrome, martin-bell syndrome, fragile x mental retardation syndrome, x-linked mental retardation and macro-orchidism, mental retardation, x-linked.