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The Journal of Clinical Endocrinology and Metabolism|November 1, 1995
Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excessR C Wilson, M D Harbison, Z S Krozowski, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 1998
A genetic defect resulting in mild low-renin hypertensionR C Wilson, S Dave-Sharma, J Q Wei, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excessR C Wilson, Z S Krozowski, K Li, et al.
Cancer Research|September 1, 1990
Establishment and characterization of a human adrenocortical carcinoma cell line that expresses multiple pathways of steroid biosynthesisA F Gazdar, H K Oie, C H Shackleton, et al.
Hepatology (Baltimore, Md.)|May 1, 1997
Hepatic basolateral sodium-dependent-bile acid transporter expression in two unusual cases of hypercholanemia and in extrahepatic biliary atresiaB L Shneider, V L Fox, K B Schwarz, et al.
European Journal of Endocrinology|November 8, 2012
Novel H6PDH mutations in two girls with premature adrenarche: 'apparent' and 'true' CRD can be differentiated by urinary steroid profilingG G Lavery, J Idkowiak, M Sherlock, et al.
The American Journal of Clinical Nutrition|May 1, 1997
Effect of psyllium in hypercholesterolemia at two monounsaturated fatty acid intakesD J Jenkins, T M Wolever, E Vidgen, 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.
Hepatology (Baltimore, Md.)|July 1, 1997
Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneityL N Bull, V E Carlton, N L Stricker, et al.
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