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American Journal of Human Genetics|July 31, 1998
Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase geneH R Waterham, F A Wijburg, R C Hennekam, et al.British Journal of Clinical Pharmacology|September 2, 1998
Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjectsS A Ridge, J Sludden, O Brown, et al.Magnetic Resonance in Medicine|October 25, 2001
beta-Ureidopropionase deficiency: a novel inborn error of metabolism discovered using NMR spectroscopy on urineS H Moolenaar, G Göhlich-Ratmann, U F Engelke, et al.Pharmacogenetics|January 26, 1999
Nomenclature for human DPYD allelesH L McLeod, E S Collie-Duguid, P Vreken, et al.American Journal of Human Genetics|August 27, 1998
Dihydropyrimidinase deficiency: structural organization, chromosomal localization, and mutation analysis of the human dihydropyrimidinase geneN Hamajima, M Kouwaki, P Vreken, et al.Human Genetics|March 10, 1999
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiencyA B Van Kuilenburg, P Vreken, N G Abeling, et al.Pageof 5