Research of Eem Syndrome has been linked to Dystrophy, Ectodermal Dysplasia, Ectrodactyly, Dysplasia, Age Related Macular Degeneration. The study of Eem Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Eem Syndrome include Pigmentation, Hair Follicle Morphogenesis, Limb Development. These pathways complement our catalog of research reagents for the study of Eem Syndrome including antibodies and ELISA kits against P-CADHERIN, CDH3, CDH15, RPE65, UVRAG.
Eem 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 Eem Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 119 products for the study of Eem Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.