Research of Branchio-oto-renal Syndrome has been linked to Complete Hearing Loss, Branchiooculofacial Syndrome, Branchioma, Dysplasia, Pathologic Fistula. The study of Branchio-oto-renal Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Branchio-oto-renal Syndrome include Localization, Pathogenesis, Ear Development, Inner Ear Development, Transport. These pathways complement our catalog of research reagents for the study of Branchio-oto-renal Syndrome including antibodies and ELISA kits against EYA1, CDCA8, SIX1, TFAP2A, LACRIMAL.
Branchio-oto-renal 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 Branchio-oto-renal Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 466 products for the study of Branchio-oto-renal Syndrome that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Chromatin Immunoprecipitation (ChIP) from our catalog of antibodies and ELISA kits.
Branchio-oto-renal Syndrome is also known as Bor Syndrome, Bor Syndromes, Branchio Oto Renal Syndrome, Branchio-oto-renal Syndromes, Branchio-otorenal Syndrome.
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