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N Moghrabi

Showing results (1-10 of 22) with videos related to

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Trends in Endocrinology and Metabolism: TEM|April 15, 2008
17beta-hydroxysteroid dehydrogenases: physiological roles in health and diseaseN Moghrabi, S Andersson
Steroids|January 1, 1997
Physiology and molecular genetics of 17 beta-hydroxysteroid dehydrogenasesS Andersson, N Moghrabi
Human Molecular Genetics|August 1, 1993
Three MspI polymorphisms at the UGT1 locusN Moghrabi, M Boxer, B Burchell
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Cell type-specific expression of 17 beta-hydroxysteroid dehydrogenase type 2 in human placenta and fetal liverN Moghrabi, J R Head, S Andersson
Experimental Eye Research|November 1, 1995
Canine homolog and exclusion of retinal degeneration slow (rds) as the gene for early retinal degeneration (erd) in the dogW N Moghrabi, W Kedzierski, G H Travis
Genomics|October 1, 1993
Identification of an A-to-G missense mutation in exon 2 of the UGT1 gene complex that causes Crigler-Najjar syndrome type 2N Moghrabi, D J Clarke, M Boxer, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Assignment of the human peroxisomal palmitoyl-CoA oxidase gene to chromosome 17q23-qter by PCR techniqueN N Moghrabi, D B Dawson, M J Bennett
American Journal of Human Genetics|September 1, 1993
Cosegregation of intragenic markers with a novel mutation that causes Crigler-Najjar syndrome type I: implication in carrier detection and prenatal diagnosisN Moghrabi, D J Clarke, B Burchell, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Deleterious missense mutations and silent polymorphism in the human 17beta-hydroxysteroid dehydrogenase 3 gene (HSD17B3)N Moghrabi, I A Hughes, A Dunaif, et al.
Annals of Human Genetics|May 1, 1992
Chromosomal assignment of human phenol and bilirubin UDP-glucuronosyltransferase genes (UGT1A-subfamily)N Moghrabi, L Sutherland, R Wooster, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Trends in Endocrinology and Metabolism: TEM|April 15, 2008
17beta-hydroxysteroid dehydrogenases: physiological roles in health and diseaseN Moghrabi, S Andersson
Steroids|January 1, 1997
Physiology and molecular genetics of 17 beta-hydroxysteroid dehydrogenasesS Andersson, N Moghrabi
Human Molecular Genetics|August 1, 1993
Three MspI polymorphisms at the UGT1 locusN Moghrabi, M Boxer, B Burchell
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Cell type-specific expression of 17 beta-hydroxysteroid dehydrogenase type 2 in human placenta and fetal liverN Moghrabi, J R Head, S Andersson
Experimental Eye Research|November 1, 1995
Canine homolog and exclusion of retinal degeneration slow (rds) as the gene for early retinal degeneration (erd) in the dogW N Moghrabi, W Kedzierski, G H Travis
Genomics|October 1, 1993
Identification of an A-to-G missense mutation in exon 2 of the UGT1 gene complex that causes Crigler-Najjar syndrome type 2N Moghrabi, D J Clarke, M Boxer, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Assignment of the human peroxisomal palmitoyl-CoA oxidase gene to chromosome 17q23-qter by PCR techniqueN N Moghrabi, D B Dawson, M J Bennett
American Journal of Human Genetics|September 1, 1993
Cosegregation of intragenic markers with a novel mutation that causes Crigler-Najjar syndrome type I: implication in carrier detection and prenatal diagnosisN Moghrabi, D J Clarke, B Burchell, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Deleterious missense mutations and silent polymorphism in the human 17beta-hydroxysteroid dehydrogenase 3 gene (HSD17B3)N Moghrabi, I A Hughes, A Dunaif, et al.
Annals of Human Genetics|May 1, 1992
Chromosomal assignment of human phenol and bilirubin UDP-glucuronosyltransferase genes (UGT1A-subfamily)N Moghrabi, L Sutherland, R Wooster, et al.
Pageof 3