Research of Smith-lemli-opitz Syndrome has been linked to Congenital Abnormality, Microcephaly, Growth Disorders, Syndactyly, Multiple Congenital Anomalies. The study of Smith-lemli-opitz Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Smith-lemli-opitz Syndrome include Pathogenesis, Transport, Cholesterol Homeostasis, Secretion, Excretion. These pathways complement our catalog of research reagents for the study of Smith-lemli-opitz Syndrome including antibodies and ELISA kits against RSH, CHONDRODYSPLASIA, STEROID SULFATASE, SMOOTHENED, AFP.
Smith-lemli-opitz 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 Smith-lemli-opitz Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 655 products for the study of Smith-lemli-opitz Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Smith-lemli-opitz Syndrome is also known as smith-lemli-opitz syndrome, rsh syndrome, slo syndrome, rutledge lethal multiple congenital anomaly syndrome, smith-lemli-opitz syndrome, type ii, smith-opitz-inborn syndrome.