JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.91, no.9, pp.3451-3456, 2006 (SCI-Expanded)
Context: Because many women with 21-hydroxylase (21-OH)-deficient nonclassic adrenal hyperplasia (NCAH) carry at least one allele affected by a severe mutation of CYP21, they are at risk for giving birth to infants with classic adrenal hyperplasia (CAH).