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Emanuel Syndrome: Disease Bioinformatics

Research of Emanuel Syndrome has been linked to Trisomy, Congenital Heart Defects, Cleft Palate, Muscle Hypotonia, Partial Trisomy. The study of Emanuel Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Emanuel Syndrome include Meiosis, Meiosis Ii. These pathways complement our catalog of research reagents for the study of Emanuel Syndrome including antibodies and ELISA kits against TBX1, CRAT, GLYAT, CAT, TBXAS1.

Emanuel 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 Emanuel Syndrome below! For more information on how to use Laverne, please read the How to Guide.

Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 835 products for the study of Emanuel Syndrome that can be applied to Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

SLC25A10 Antibody

NBP1-85214