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Trends in Endocrinology and Metabolism: TEM|August 1, 1992
Disorders of steroid 11 beta-hydroxylase isozymesP C White, L PascoeHypertension (Dallas, Tex. : 1979)|June 1, 1996
Apparent mineralocorticoid excess: genotype is correlated with biochemical phenotypeT Mune, P C WhiteThe Journal of Steroid Biochemistry and Molecular Biology|April 1, 1993
Mutations in human 11 beta-hydroxylase genes: 11 beta-hydroxylase deficiency in Jews of Morocco and corticosterone methyl-oxidase II deficiency in Jews of IranA Rösler, P C WhiteInternational Journal of Clinical Pharmacology, Therapy, and Toxicology|November 1, 1986
Note on the enzyme assay for urinary D-glucaric acid and correlation with rifampicin-induced mixed function oxidase activityW Perry, M V JenkinsMethods in Molecular Medicine|February 23, 2011
Detection of mutations causing hemophilia a using an in vitro coupled transcription and translation systemC Ononye, P V JenkinsMethods in Molecular Medicine|February 23, 2011
Inversion mutation analysis in hemophilia a by restriction enzyme analysis and southern blottingC Ononye, P V JenkinsInternational Journal of Clinical Pharmacology, Therapy, and Toxicology|January 1, 1987
Plasma gamma glutamyltransferase levels during rifampicin therapy for tuberculosisW Perry, M V JenkinsInternational Journal of Clinical Pharmacology, Therapy, and Toxicology|July 1, 1986
Hepatic mixed function oxidase induction during rifampicin/isoniazid therapy in Indian vegetariansW Perry, M V JenkinsPediatrics|September 5, 2001
Improving management of diabetic ketoacidosis in childrenE I Felner, P C WhiteThe Journal of Reproductive Medicine|January 1, 1984
Clinical significance of fetal heart rate patterns during labor. VIII. Breech presentationsP C White, L A CibilsPageof 29