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Reagents, Molecular Assay, Gene Anomaly, Mutation, ALX4

Definition : Molecular assay reagents intended to identify mutations in the aristaless-like homeobox 4 (ALX4) gene, located at chromosome 11p11.2, which is believed to be a transcription factor involved in skull and limb development. Mutations at this locus have been identified in patients with enlarged parietal foramina type 2.

Entry Terms : "Multiple Exostoses Gene Mutation Detection Reagents" , "Deletion Contiguous Syndrome with Multiple Exostoses Gene Mutation Detection Reagents" , "Cranium Bifidum Syndrome Gene Mutation Detection Reagents" , "Enlarged Parietal Foramina Type 2 Gene Mutation Detection Reagents" , "ALX4 Gene Mutation Detection Reagents"

UMDC code : 24286

   

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