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  • 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.
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