Weaver Syndrome is a congenital disorder that causes overgrowth. The accelerated growth is during the pre and postnatal maturation periods of a child. The symptoms of Weaver Syndrome include broad face, deep set nails, and eyes that are far apart. Weaver Syndrome is still being studied.
Weaver 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 Weaver Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 679 products for the study of Weaver Syndrome that can be applied to Chromatin Immunoprecipitation, Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Chromatin Immunoprecipitation (ChIP), Immunohistochemistry from our catalog of antibodies and ELISA kits.
Weaver Syndrome is also known as weaver syndrome, mental retardation, microcephaly, weight deficiency, unusual facies, clinodactyly, bone hypoplasia, and cleft palate, overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly, weaver williams syndrome, weaver-williams syndrome, weaver smith syndrome, weaver like syndrome, weaver-like syndrome, wss.