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Biomedical Mass Spectrometry|March 1, 1981
Two new sulphur-containing amino acids in manR J Truscott, D Malegan, E McCairns, et al.Lancet (London, England)|November 28, 1992
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.Pediatrics|October 1, 1982
beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformationsG K Brown, S M Hunt, R Scholem, et al.Acta Neuropathologica|January 1, 1988
Neuropathology in glutaric acidaemia type 1C W Chow, E A Haan, S I Goodman, et al.American Journal of Medical Genetics|January 1, 1981
Further delineation of the C (trigonocephaly) syndromeR M Antley, D S Hwang, W Theopold, et al.Human Molecular Genetics|May 23, 1998
Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxicationE P Treacy, B R Akerman, L M Chow, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|March 5, 1981
New metabolites in isovaleric acidemiaR J Truscott, D Malegan, E McCairns, et al.Pageof 19