Research of 1p36 Deletion Syndrome has been linked to Monosomy, Cytogenetic Abnormality, Muscle Hypotonia, Congenital Heart Defects, Epilepsy. The study of 1p36 Deletion Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to 1p36 Deletion Syndrome include Cell Cycle, Tube Development, Tooth Eruption, Membrane Repolarization, Associative Learning. These pathways complement our catalog of research reagents for the study of 1p36 Deletion Syndrome including antibodies and ELISA kits against NT5C3, ANXA2, SKI, MB, KCNAB2.
1p36 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 1p36 Deletion Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 619 products for the study of 1p36 Deletion Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.