Research of Fryns Syndrome has been linked to Diaphragmatic Hernia, Hernia, Hypoplasia, Congenital Abnormality, Congenital Diaphragmatic Hernia. The study of Fryns Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Fryns Syndrome include Pathogenesis, Ossification, Neural Crest Cell Development, Cell Development, Lung Development. These pathways complement our catalog of research reagents for the study of Fryns Syndrome including antibodies and ELISA kits against GLUCOCEREBROSIDASE, CHONDRODYSPLASIA, COUP-TFII, E11, DU.
Fryns 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 Fryns Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 415 products for the study of Fryns Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.