Research of De Barsy Syndrome has been linked to Cutis Laxa, Muscle Hypotonia, Progeria, Growth Retardation, Dwarfism. The study of De Barsy Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to De Barsy Syndrome include Cell Proliferation, Translation, Pathogenesis. These pathways complement our catalog of research reagents for the study of De Barsy Syndrome including antibodies and ELISA kits against ATHETOID, NEUTROPHILIC ELASTASE, ARSA, ELN, FBN1.
De Barsy 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 De Barsy Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 851 products for the study of De Barsy Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.
De Barsy Syndrome is also known as de barsy syndrome, corneal clouding, cutis laxa and mental retardation, cutis laxa growth deficiency syndrome, progeroid syndrome, de barsy type, progeroid syndrome of de barsy.