Research of Fetal Warfarin Syndrome has been linked to Embryopathies, Chondrodysplasia Punctata, Pregnancy Complications, Cardiovascular, Hemorrhage, Hypoplasia. The study of Fetal Warfarin Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Fetal Warfarin Syndrome include Pathogenesis, Cartilage Development, Regeneration, Cell Division, Coagulation. These pathways complement our catalog of research reagents for the study of Fetal Warfarin Syndrome including antibodies and ELISA kits against CHONDRODYSPLASIA, BGLAP, GLA, NAT8, ARSE.
Top Research Reagents
We have 735 products for the study of Fetal Warfarin Syndrome that can be applied to Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Fetal Warfarin Syndrome is also known as Congenital Warfarin Syndrome, Coumarin Syndrome, Foetal Warfarin Syndrome, Warfarin Embryopathy, Warfarin Syndrome.