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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.
Vizit™, under license from BioVista Inc.

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.

Related Genes

Grebe Syndrome has been researched against:

Related Pathways

Related PTMs

Alternate Names

Grebe Syndrome is also known as Grebe Chondrodysplasia, Grebe Dysplasia.