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The Journal of Clinical Endocrinology and Metabolism|January 1, 1996
Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiencyS Andersson, W M Geissler, L Wu, et al.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.
The Journal of Clinical Endocrinology and Metabolism|July 14, 1998
Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excessS Dave-Sharma, R C Wilson, M D Harbison, et al.
American Journal of Human Genetics|June 13, 1998
DAX1 mutations map to putative structural domains in a deduced three-dimensional modelY H Zhang, W Guo, R L Wagner, et al.
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