Research of Charge Syndrome has been linked to Congenital Ocular Coloboma (disorder), Choanal Atresia, Congenital Heart Defects, Atresia, Congenital Abnormality. The study of Charge Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Charge Syndrome include Pathogenesis, Chromatin Remodeling, Neurogenesis, Cell Proliferation, Atp-dependent Chromatin Remodeling. These pathways complement our catalog of research reagents for the study of Charge Syndrome including antibodies and ELISA kits against STRABISMUS, SEVERE COMBINED IMMUNODEFICIENCY, STS, BMP4, CHD2.
Charge 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 Charge Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 723 products for the study of Charge Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Chromatin Immunoprecipitation (ChIP) from our catalog of antibodies and ELISA kits.