Research of Roberts-sc Phocomelia Syndrome has been linked to Craniofacial Abnormalities, Cleft Palate, Growth Retardation, Cytogenetic Abnormality, Cleft Lip. The study of Roberts-sc Phocomelia Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Roberts-sc Phocomelia Syndrome include Centromere Separation, Sister Chromatid Cohesion, Chromosome Segregation, Metaphase, Cell Cycle. These pathways complement our catalog of research reagents for the study of Roberts-sc Phocomelia Syndrome including antibodies and ELISA kits against STRABISMUS, ARR3, DDX11, DNAH5, ERCC2.
Top Research Reagents
We have 1487 products for the study of Roberts-sc Phocomelia Syndrome that can be applied to Chromatin Immunoprecipitation, Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Roberts-sc Phocomelia Syndrome is also known as Hypomelia-hypotrichosis-facial Hemangioma Syndrome, Pseudothalidomide Syndrome, Robert's Syndrome, Roberts Syndrome.