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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.
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.
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.
Science (New York, N.Y.)|November 13, 1987
Real-time landslide warning during heavy rainfallD K Keefer, R C Wilson, R K Mark, et al.
The Plant Cell|January 15, 2000
The ROOT MERISTEMLESS1/CADMIUM SENSITIVE2 gene defines a glutathione-dependent pathway involved in initiation and maintenance of cell division during postembryonic root developmentT Vernoux, R C Wilson, K A Seeley, et al.
The Journal of Antimicrobial Chemotherapy|January 29, 2026
Exploring the opportunity for therapeutic drug monitoring (TDM) and precision dose antimicrobials in an outpatient antimicrobial therapy (OPAT) service: a prospective observational studyR C Wilson, M J Gilchrist, R Cele, et al.
Developmental Biology|June 19, 1998
The cloche and spadetail genes differentially affect hematopoiesis and vasculogenesisM A Thompson, D G Ransom, S J Pratt, 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.
BJOG : an International Journal of Obstetrics and Gynaecology|September 20, 2018
Associations between maternal physical activity in early and late pregnancy and offspring birth size: remote federated individual level meta-analysis from eight cohort studiesS Pastorino, T Bishop, S R Crozier, et al.
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