Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Deletion, NR0B1

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Deletion, NR0B1

Definition : Molecular assay reagents intended to identify deletions in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene, located in Xp21.3-p21.2. Inherited genetic deletions are present in male patients with adrenal hypoplasia congenita. Most males are infertile; carrier females may have symptoms of adrenal insufficiency and/or hypogonadotropic hypogonadism.

Entry Terms : "X-Linked Adrenal Hypoplasia Congenita Diagnostic Reagents" , "Congenital Adrenal Hypoplasia Diagnostic Reagents" , "NR0B1 Gene Deletion Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Deletion, NR0B1"

UMDC code : 24186

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