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C H Shackleton

Showing results (171-180 of 175) with videos related to

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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.
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 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.
Pageof 18

Showing results (171-180 of 175) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 175 results.
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.
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 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.
Pageof 18