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Merke DP, Bornstein SR (2005) Congenital adrenal hyperplasia. <i>Lancet <\/i>365: 2125-2136.","DOI":"10.1016\/S0140-6736(05)66736-0"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Speiser PW, White PC (2003) Congenital adrenal hyperplasia. <i>N Engl J Med <\/i>349: 776-788.","DOI":"10.1056\/NEJMra021561"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Deneux C, Tardy V, Dib A, Mornet E, Billaud L, et al. (2001) Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.<i> J Clin Endocrinol Metab<\/i> 86: 207-213.","DOI":"10.1210\/jcem.86.1.7131"},{"key":"4","unstructured":"4. Tajima T, Fujikura K, Fukushi M, Hotsubo T, Mitsuhashi Y (2012) Neonatal screening for congenital adrenal hyperplasia in Japan. <i>Pediatr Endocrinol Rev <\/i>10 Suppl 1: 72-78."},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Tajima T, Fujieda K, Nakae J, Toyoura T, Shimozawa K, et al. (1997) Molecular basis of nonclassical steroid 21-hydroxylase deficiency detected by neonatal mass screening in Japan. <i>J Clin Endocrinol Metab<\/i> 82: 2350-2356.","DOI":"10.1210\/jcem.82.7.4094"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Tajima T, Fujieda K, Nakae J, Mikami A, Cutler GB Jr (1998) Mutations of the CYP21 gene in nonclassical steroid 21-hydroxylase deficiency in Japan. <i>Endocr J<\/i> 45: 493-497.","DOI":"10.1507\/endocrj.45.493"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Kashimada K, Ono M, Onishi T, Koyama S, Toyoura T, et al. (2008) Clinical course of patients with nonclassical 21-hydroxylase deficiency (21-OHD) diagnosed in infancy and childhood. <i>Endocr J<\/i> 55: 397-404.","DOI":"10.1507\/endocrj.K07E-057"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Nagasaki K, Usui T, Asami T, Ogawa Y, Kikuchi T, et al. (2009) H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency. <i>Clin Pediatr Endocrinol<\/i> 18: 111-113.","DOI":"10.1297\/cpe.18.111"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Homma K, Hasegawa T, Takeshita E, Watanabe K, Anzo M, et al. (2004) Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates. <i>J Clin Endocrinol Metab<\/i> 89: 6087-6091.","DOI":"10.1210\/jc.2004-0473"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Kusuda S, Tachibana K, Saisho S, Yokota I, Igarashi Y, et al. (1999) Guideline for the Treatment of Patients with 21-OHase Deficiency Detected by Neonatal Screening (Revised in 1999). <i>Clin Pediatr Endocrinol<\/i> 8: 61-65.","DOI":"10.1297\/cpe.8.61"},{"key":"11","unstructured":"11. Speiser PW, Dupont B, Rubinstein P, Piazza A, Kastelan A, et al. (1985) High frequency of nonclassical steroid 21-hydroxylase deficiency. <i>Am J Hum Genet<\/i> 37: 650-667."},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Weintrob N, Brautbar C, Pertzelan A, Josefsberg Z, Dickerman Z, et al. (2000) Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency. <i>Eur J Endocrinol <\/i>143: 397-403.","DOI":"10.1530\/eje.0.1430397"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. White PC, Speiser PW (2000) Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. <i>Endocr Rev<\/i> 21: 245-291.","DOI":"10.1210\/er.21.3.245"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. New MI (2006) Extensive clinical experience: nonclassical 21-hydroxylase deficiency. <i>J Clin Endocrinol Metab<\/i> 91: 4205-4214.","DOI":"10.1210\/jc.2006-1645"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. New MI, Lorenzen F, Lerner AJ, Kohn B, Oberfield SE, et al. (1983) Genotyping steroid 21-hydroxylase deficiency: hormonal reference data. <i>J Clin Endocrinol Metab<\/i> 57: 320-326.","DOI":"10.1210\/jcem-57-2-320"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Speiser PW, Azziz R, Baskin LS, Ghizzoni L, Hensle TW, et al. 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