Research of 22q11 Deletion Syndrome has been linked to Digeorge Syndrome, Schizophrenia, Congenital Heart Defects, 22q11 Partial Monosomy Syndrome, Mental Disorders. The study of 22q11 Deletion Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to 22q11 Deletion Syndrome include Pathogenesis, Prepulse Inhibition, Cognition, Brain Development, Neural Crest Cell Development. These pathways complement our catalog of research reagents for the study of 22q11 Deletion Syndrome including antibodies and ELISA kits against COMT, TBX1, PRODH, SS18L1, FGF8.
22q11 Deletion 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 22q11 Deletion Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 920 products for the study of 22q11 Deletion Syndrome that can be applied to Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.