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Grebe Syndrome: Disease Bioinformatics
Grebe syndrome is a very rare form of short-limbed dwarfism. It is a genetic condition, passed by autosomal recessive inheritance. It is characterized by shortening of all the four limbs. The affected baby has normal intelligence and normal life span.
Grebe 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 Grebe Syndrome below!
For more information on how to use Laverne, please read the How to Guide
Top Research Reagents
We have 20 products for the study of Grebe Syndrome that can be applied to Western Blot, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Grebe Syndrome has been researched against:
Grebe Syndrome has been studied in relation to diseases such as:
Alternate NamesGrebe Syndrome is also known as Grebe Chondrodysplasia, Grebe Dysplasia.