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Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias: Disease Bioinformatics

Research of Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias has been linked to Hypospadias, Polydactyly, Congenital Hand Deformities, Single Gene Defect, Congenital Foot Deformity. The study of Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias including antibodies and ELISA kits against HOXA13.

Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias 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 Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 1 product for the study of Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias that can be applied to various Western Blot from our catalog of antibodies and ELISA kits.

H00003209-Q01
SDS-Page: Recombinant Human HOXA13 Protein [H00003209-Q01] - 12.5% SDS-PAGE Stained with Coomassie Blue.


Species Human


Related Genes

Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias has been researched against:

Related Diseases

Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias has been studied in relation to diseases such as:

Alternate Names

Autosomal Dominant Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias is also known as Guttmacher Syndrome.