Research of Congenital Contractural Arachnodactyly has been linked to Arachnodactyly, Marfanoid Joint Hypermobility Syndrome, Marfan Syndrome, Muscle Contracture, Connective Tissue Diseases. The study of Congenital Contractural Arachnodactyly has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Congenital Contractural Arachnodactyly include Pathogenesis, Gastrulation, Tissue Morphogenesis, Convergent Extension, Osteoblast Differentiation. These pathways complement our catalog of research reagents for the study of Congenital Contractural Arachnodactyly including antibodies and ELISA kits against TRANSFORMING GROWTH FACTOR-BETA TYPE II RECEPTOR, FBN-2, FBN-1, BRCA1, EGF.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Congenital Contractural Arachnodactyly below!
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We have 750 products for the study of Congenital Contractural Arachnodactyly that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Congenital Contractural Arachnodactyly is also known as congenital contractural arachnodactyly, ear anomalies-contractures-dysplasia of bone with kyphoscoliosis, marfanoid hypermobility syndrome, hecht syndrome (disorder), arachnodactyly.