Research of Acrocephalosyndactylia has been linked to Apert Syndrome, Craniosynostosis, Craniofacial Dysostosis, Syndactyly, Congenital Abnormality. The study of Acrocephalosyndactylia has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Acrocephalosyndactylia include Pathogenesis, Ossification, Osteoblast Differentiation, Cell Proliferation, Transposition. These pathways complement our catalog of research reagents for the study of Acrocephalosyndactylia including antibodies and ELISA kits against STRABISMUS, BGLAP, RUNX2, FGF2, FGF10.
Top Research Reagents
We have 2230 products for the study of Acrocephalosyndactylia that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Acrocephalosyndactylia is also known as acrocephalosyndactylia, acrocephalosyndactyly (apert), acrocephaly, acs ii, syndactylic oxycephaly, apert-crouzon disease, vogt cephalodactyly, acs 1, acs1.