Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, MSX2

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, MSX2

Definition : Molecular assay reagents intended to identify mutations in the muscle segment homeo box homologue 2 (MSX2) gene, located at chromosome 5q34-q35, which encodes for a transcription factor protein presumed to be critical for skull development. Mutations at this locus have been identified in patients with parietal foramina type 1 and craniosyostosis type 2.

Entry Terms : "Familial Craniosynostosis Type 2 Gene Mutation Reagents" , "Cranium Bifidum Syndrome Gene Mutation Reagents" , "Enlarged Parietal Foramina Type 1 Gene Mutation Reagents" , "MSX2 Gene Mutation Detection Reagents" , "IVD Test Reagent/Kits, Molecular Assay, Tumor Marker, Gene Mutation, hML1/hMSH2" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, MSX2"

UMDC code : 24614

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