Research of Holt-oram Syndrome has been linked to Congenital Heart Defects, Congenital Hand Deformities, Heart Septal Defects, Atrial Septal Defects, Heart Diseases. The study of Holt-oram Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Holt-oram Syndrome include Localization, Pathogenesis, Limb Development, Heart Development, Cardiac Conduction. These pathways complement our catalog of research reagents for the study of Holt-oram Syndrome including antibodies and ELISA kits against ATRIAL NATRIURETIC FACTOR, BMP4, NKX2-5, GATA4, GJA5.
Holt-oram 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 Holt-oram Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 691 products for the study of Holt-oram Syndrome that can be applied to Western Blot, Flow Cytometry, Chromatin Immunoprecipitation, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Chromatin Immunoprecipitation (ChIP) from our catalog of antibodies and ELISA kits.
Holt-oram Syndrome is also known as holt-oram syndrome, heart-hand syndrome, type 1, ventriculo-radial syndrome, atriodigital dysplasia, cardiac-limb syndrome, hos, atrio-digital syndrome, atrio digital syndrome, heart-hand syndrome, hearthand syndrome, holt oram syndrome, hos 1.