Research of Adams Oliver Syndrome has been linked to Aplasia, Nos, Limb Deformities, Congenital, Aplasia Cutis Congenita, Ectodermal Dysplasia, Limb Defect. The study of Adams Oliver Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Adams Oliver Syndrome include Pathogenesis, Regeneration, Vasculogenesis, Cell Adhesion, Actin Cytoskeleton Organization. These pathways complement our catalog of research reagents for the study of Adams Oliver Syndrome including antibodies and ELISA kits against GROWTH HORMONE, RHO GTPASE-ACTIVATING PROTEIN 31, STRABISMUS, ACACA, CDC42.
Top Research Reagents
We have 1330 products for the study of Adams Oliver Syndrome that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Adams Oliver Syndrome is also known as adams oliver syndrome, aos, aplasia cutis congenita with terminal transverse defects of limbs, and skull defects, congenital scalp defects with distal limb anomalies, scalp defects with ectrodactyly, limb scalp and skull defects, forrest h adams syndrome, scalp and head syndrome.