Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, FGFR2

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, FGFR2

Definition : Molecular assay reagents intended to identify mutations in the fibroblast growth factor receptor 2 (FGFR2) gene, located at chromosome 10q26, which encodes for acidic and basic fibroblast growth factor receptors. Mutations at this locus have been identified in patients with hereditary defects in the normal ossification of fetal cranial cartilages (craniofacial dysostosis), including several different but related diseases such as Apert's syndrome, Beare-Stevenson cutis gyrata syndrome, Crouzon syndrome, Pfeiffer's syndrome (variants 1, 2, and 3), and Jackson-Weiss syndrome.

Entry Terms : "FGFR2-Related Isolated Coronal Synostosis Gene Mutation Detection Reagents" , "Crouzon Syndrome Gene Mutation Detection Reagents" , "Beare-Stevenson Syndrome Gene Mutation Detection Reagents" , "Apert Syndrome Gene Mutation Detection Reagents" , "Acrocephalosyndactyly Gene Mutation Detection Reagents" , "FGFR 2-Related Craniosynostosis Gene Mutation Detection Reagents" , "Jackson-Weiss Syndrome Gene Mutation Detection Reagents" , "Pfeiffer Syndrome Gene Mutation Detection Reagents" , "Craniosynostosis Gene Mutation Detection Reagents" , "FGFR2 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, FGFR2"

UMDC code : 24429

Filters
Manufacturers
Distributors
U.S.companies only
Suppress Subsidiary Companies
   

1-1 of 1 Match(es).

ACROBiosystems Inc

Company Type: Parent

1-1 of 1 Match(es).