Submit your image related to Diseases to be featured!
Submit your Twitter account related to Barber-say Syndrome to be featured!
Submit your blog on Barber-say Syndrome to be featured!
||Submit your event on Barber-say Syndrome to be featured!
Submit your video on Barber-say Syndrome to be featured!
Submit your charity on Barber-say Syndrome to be featured!
Barber-say Syndrome: Disease Bioinformatics
Barber-say Syndrome is an extremely rare condition that is associated with excessive hair growth, a large mouth, outward turned eyelids, and fragile skin. Barber-say Syndrome has only been noted in 20 people and is an inherited condition that is autosomal recessive. Because of its rare diagnosis, there is limited information on Barber-say Syndrome.
Barber-say 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 Barber-say Syndrome below!
For more information on how to use Laverne, please read the How to Guide
Top Research Reagents
We have 68 products for the study of Barber-say Syndrome that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Applications WB, Flow, IHC
Barber-say Syndrome has been researched against:
Barber-say Syndrome has been linked to:
Barber-say Syndrome has been studied in relation to diseases such as:
Alternate NamesBarber-say Syndrome is also known as barber say syndrome, hypertrichosis, atrophic skin, ectropion, and macrostomia, hypertrichosis atrophic skin ectropion macrostomia.