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.
Top Research Reagents
We have 1691 products for the study of Saethre-chotzen Syndrome that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot 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.