Research of Cat Eye Syndrome has been linked to Congenital Ocular Coloboma (disorder), Cytogenetic Abnormality, Anus, Imperforate, Extra Unidentified Structurally Abnormal Chromosom, Trisomy. The study of Cat Eye Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Cat Eye Syndrome include Localization, Metaphase, Interphase, Cell Proliferation, Development Of Secondary Sexual Characteristics. These pathways complement our catalog of research reagents for the study of Cat Eye Syndrome including antibodies and ELISA kits against CRAT, CAT, GLYAT, TBX1, CECR1.
Cat Eye 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 Cat Eye Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 652 products for the study of Cat Eye Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Cat Eye Syndrome is also known as cat eye syndrome, chromosome 22 partial tetrasomy, opitz trigonocephaly syndrome, schmid-fraccaro syndrome, ces, inv dup(22)(q11), c syndrome.
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