Research of Saethre-chotzen Syndrome has been linked to Acrocephalosyndactylia, Craniosynostosis, Congenital Abnormal Synostosis, Syndactyly, Blepharoptosis. The study of Saethre-chotzen Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Saethre-chotzen Syndrome include Osteoblast Differentiation, Ossification, Localization, Cell Growth, Limb Development. These pathways complement our catalog of research reagents for the study of Saethre-chotzen Syndrome including antibodies and ELISA kits against BGLAP, RUNX2, CDKN1A, CDKN2B, FGFR1.
Saethre-chotzen 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 Saethre-chotzen Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 802 products for the study of Saethre-chotzen Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Chromatin Immunoprecipitation (ChIP), Immunohistochemistry from our catalog of antibodies and ELISA kits.
Saethre-chotzen Syndrome is also known as saethre-chotzen syndrome, acrocephaly, skull asymmetry, and mild syndactyly, chotzen syndrome, dysostosis craniofacialis with hypertelorism, acrocephalosyndactyly, type iii, acrocephalosyndactyly type iii, acrocephalosyndactyly iii, hemoglobin sc disease, acrocephaly, dysostoses, acs iii, acs 3.