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Developmental Pharmacology and Therapeutics|January 1, 1981
Ascorbic acid treatment in nephropathic cystinosis in identical twinsS E Oberfield, L S Levine, D Wellner, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1995
Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase geneR C Wilson, J Q Wei, K C Cheng, et al.
Recent Progress in Hormone Research|January 1, 1994
Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridizationP W Speiser, P C White, J Dupont, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiencyA B Mercado, R C Wilson, K C Cheng, et al.
Therapeutic Drug Monitoring|January 1, 1986
Microfilter paper method for antipyrine determination in whole blood by high pressure liquid chromatographyS Loche, A B Rifkind, E Stoner, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 1995
Molecular basis of human 3 beta-hydroxysteroid dehydrogenase deficiencyJ Simard, E Rheaume, F Mebarki, et al.
Clinical Endocrinology|January 1, 1986
Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect?E Stoner, J Dimartino-Nardi, U Kuhnle, et al.
Pediatric Research|September 1, 1980
Aldosterone response to prolonged ACTH infusion in juvenile hypertensionW Rauh, K Gottesdiener, D Chow, et al.
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