Research of Shprintzen-goldberg Syndrome has been linked to Marfan Syndrome, Craniosynostosis, Arachnodactyly, Congenital Heart Defects, Aneurysm. The study of Shprintzen-goldberg Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Shprintzen-goldberg Syndrome include System Development, Response To Anesthetic, Nervous System Development, Central Nervous System Development, Pathogenesis. These pathways complement our catalog of research reagents for the study of Shprintzen-goldberg Syndrome including antibodies and ELISA kits against TRANSFORMING GROWTH FACTOR-BETA TYPE II RECEPTOR, STRABISMUS, ALDH9A1, COL3A1, CYP17A1.
Shprintzen-goldberg 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 Shprintzen-goldberg Syndrome below!
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We have 630 products for the study of Shprintzen-goldberg 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.
Shprintzen-goldberg Syndrome is also known as shprintzen-goldberg syndrome, shprintzen-goldberg craniosynostosis syndrome, shprintzen-goldberg marfanoid syndrome, marfanoid-craniosynostosis syndrome, craniosynostosis with arachnodactyly and abdominal hernias, marfanoid disorder with craniosynostosis type 1, marfanoid craniosynostosis syndrome.