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Hanhart's Syndrome: Disease Bioinformatics

Research of Hanhart's Syndrome has been linked to Micrognathism, Limb Deformities, Congenital, Mandibulofacial Dysostosis, Mobius Syndrome, Congenital Abnormality. The study of Hanhart's Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hanhart's Syndrome include Cell Death, Pathogenesis. These pathways complement our catalog of research reagents for the study of Hanhart's Syndrome including antibodies and ELISA kits against GPSM2.

Hanhart's 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 Hanhart's 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 8 products for the study of Hanhart's Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP1-53125
Western Blot: GPSM2 Antibody [NBP1-53125] - Sample Tissue: Human Lung Tumor Antibody Dilution: 1.0 ug/mlImmunocytochemistry/Immunofluorescence: GPSM2 Antibody [NBP1-53125] - Human cell lines.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF, IHC


Related Genes

Hanhart's Syndrome has been researched against:

Related Pathways

Hanhart's Syndrome has been linked to:

Alternate Names

Hanhart's Syndrome is also known as Hanhart Syndrome, Oromandibular Limb Hypogenesis Complex.