Research of Acrocallosal Syndrome has been linked to Congenital Absence, Agenesis Of Corpus Callosum, Polydactyly, Greig Cephalopolysyndactyly Syndrome, Orbital Separation Excessive. The study of Acrocallosal Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Acrocallosal Syndrome include Pathogenesis, Brain Development, Cell Adhesion, Dna Methylation, Autolysis. These pathways complement our catalog of research reagents for the study of Acrocallosal Syndrome including antibodies and ELISA kits against GLI3, KIF7, ACACA, STRABISMUS, ABCA4.
Acrocallosal 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 Acrocallosal Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 1044 products for the study of Acrocallosal Syndrome that can be applied to Chromatin Immunoprecipitation, Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Acrocallosal Syndrome is also known as acrocallosal syndrome, acrocallosal syndrome, schinzel type, schinzel acrocallosal syndrome, schinzel syndrome 1, absence of corpus callosum with unusual facial appearance, mental deficiency, duplication of the halluces and polydactyly, acls, acs.