Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, FOXL2

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, FOXL2

Definition : Molecular assay reagents intended to identify mutations in the forkhead box L2 (FOXL2) gene, located at chromosome 3q23, a probable transcription regulator. Mutations at this locus have been identified in patients with classic blepharophimosis syndrome (BPES); they are also associated with infertility caused by premature ovarian failure (POF).

Entry Terms : "Blepharophimosis, Ptosis, and Epicanthus Inversus Type 2 (BPES 2) Gene Mutation Detection Reagents" , "Blepharophimosis, Ptosis, and Epicanthus Inversus Type 1 (BPES 1) Gene Mutation Detection Reagents" , "Blepharophimosis, Ptosis, and Epicanthus Inversus (BPES) Gene Mutation Detection Reagents" , "Blepharophimosis Syndrome Gene Mutation Detection Reagents" , "FOXL2 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, FOXL2"

UMDC code : 24433

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Mayo Medical Laboratories

Company Type: Parent

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