Research of Freeman-sheldon Syndrome has been linked to Arthrogryposis, Craniofacial Dysostosis, Congenital Clubfoot, Congenital Hand Deformities, Dysplasia. The study of Freeman-sheldon Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Freeman-sheldon Syndrome include Transposition, Pathogenesis, Myelination. These pathways complement our catalog of research reagents for the study of Freeman-sheldon Syndrome including antibodies and ELISA kits against STRABISMUS, MYOSIN HEAVY CHAIN 3, CRINKLED, FTA, ARHGAP4.
Freeman-sheldon 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 Freeman-sheldon Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 361 products for the study of Freeman-sheldon Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Freeman-sheldon Syndrome is also known as freeman sheldon syndrome, craniocarpotarsal dysplasia, whistling face syndrome, fss, arthrogryposis, distal, type 2a, distal arthrogryposis, type 2a, distal arthrogryposis syndrome.