Research of Laurin-sandrow Syndrome has been linked to Congenital Hand Deformities, Polydactyly, Congenital Foot Deformity, Syndactyly, Congenital Abnormality. The study of Laurin-sandrow Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Laurin-sandrow Syndrome including antibodies and ELISA kits against E11, GLI3, IHH, LSS, RARB.
Laurin-sandrow 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 Laurin-sandrow Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 152 products for the study of Laurin-sandrow Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Chromatin Immunoprecipitation (ChIP), Immunohistochemistry from our catalog of antibodies and ELISA kits.
Laurin-sandrow Syndrome is also known as laurin-sandrow syndrome, fibula ulna duplication tibia radius absence, mirror hands and feet with nasal defects, tetramelic mirror-image polydactyly, laurin sandrow syndrome, sandrow syndrome.