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Pediatric Research|October 1, 1979
Malignant hyperphenylalaninemia--clinical features, biochemical findings, and experience with administration of biopterinsD M Danks, P Schlesinger, F Firgaira, et al.Lancet (London, England)|April 2, 1994
Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1D Ravine, R N Gibson, R G Walker, et al.Pediatric Research|May 1, 1989
Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patientsS J Mihalik, H W Moser, P A Watkins, et al.Human Genetics|June 1, 1994
Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemiaK Nanao, K Okamura-Ikeda, Y Motokawa, et al.Lancet (London, England)|January 19, 1991
Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.Physics in Medicine and Biology|March 1, 1992
Full data utilization in PVI using the 3D radon transformM W Stazyk, J G Rogers, R HarropJournal of Medical Genetics|April 1, 1995
Severe intrauterine growth retardation with increased mitomycin C sensitivity: a further chromosome breakage syndromeC G Woods, M Leversha, J G RogersJournal of Medical Genetics|July 1, 1994
Two sibs who are double heterozygotes for achondroplasia and pseudoachondroplastic dysplasiaC G Woods, J G Rogers, V MayneIEEE Transactions on Medical Imaging|January 1, 1987
The Theory of Three-Dimensional Image Reconstruction for PETJ G Rogers, R Harrop, P E KinahanJournal of Computer Assisted Tomography|May 1, 1985
Contribution from random coincidences to PET images: the effect of detector "wobbling"M Bergstrom, J G Rogers, B D PatePageof 19