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.
Fragile X Syndrome Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Fragile X Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 807 products for the study of Fragile X Syndrome that can be applied to Chromatin Immunoprecipitation, Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry 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.