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Acta Endocrinologica|May 1, 1978
Primary intracranial HCG-producing germinoma in a boy with congenital adrenal hyperplasiaL S Levine, M Novogroder, B Saxena, et al.The Journal of Biological Chemistry|September 5, 1991
The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localizationG M Tannin, A K Agarwal, C Monder, et al.The Journal of Clinical Investigation|May 1, 1991
A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan originP C White, J Dupont, M I New, et al.American Journal of Diseases of Children (1960)|July 1, 1987
Recurrence of Cushing's disease in childhood after radiotherapy-induced remissionM Cappa, E Stoner, J DiMartino-Nardi, et al.Clinical Endocrinology|April 1, 1984
Recovery of adrenal function after treatment of adrenocortical carcinoma with o,p'-DDDF Greig, S E Oberfield, L S Levine, et al.American Journal of Human Genetics|September 1, 1988
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequenciesC E Aston, S L Sherman, N E Morton, et al.American Journal of Human Genetics|June 1, 1988
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiencyS L Sherman, C E Aston, N E Morton, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1994
No evidence of mutations in the genes for type I and type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) in nonclassical 3 beta HSD deficiencyM Zerah, E Rhéaume, P Mani, et al.Human Genetics|December 1, 1992
Variants of the anti-Müllerian hormone gene in a compound heterozygote with the persistent Müllerian duct syndrome and his familyD Carré-Eusèbe, S Imbeaud, M Harbison, et al.Molecular Endocrinology (Baltimore, Md.)|May 1, 1991
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency alleleM T Tusie-Luna, P W Speiser, M Dumic, et al.Pageof 21