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Gene|November 21, 1996
RS cyclophilins: identification of an NK-TR1-related cyclophilinF P Nestel, K Colwill, S Harper, et al.Lancet (London, England)|September 9, 1989
Problems in genetic prediction for Huntington's diseaseM J Morris, A Tyler, L Lazarou, et al.Journal of Medical Genetics|December 1, 1989
Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markersA M Norman, J L Floyd, A L Meredith, et al.Journal of Medical Genetics|August 1, 1989
Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of WalesL A Tyfield, A L Meredith, M J Osborn, et al.Archives of Disease in Childhood|July 1, 1979
Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated casesJ R Sibert, P S Harper, R J Thompson, et al.The Science of the Total Environment|February 8, 2006
Turbidity dynamics during spring storm events in an urban headwater river system: the Upper Tame, West Midlands, UKD M Lawler, G E Petts, I D L Foster, et al.Journal of Medical Genetics|April 1, 1990
Becker muscular dystrophy: correlation of deletion type with clinical severityA M Norman, N S Thomas, H M Kingston, et al.Biochemistry International|May 1, 1984
Effect of oxygen-derived reactive species on cartilage proteoglycan-hyaluronate aggregatesE J Bates, G S Harper, D A Lowther, et al.Clinical Genetics|January 1, 1995
Risk estimates for developing motor neurone disease in first-degree relativesC M James, R G Newcombe, P S Harper, et al.Journal of Neuroscience Methods|June 27, 2017
An engineered home environment for untethered data telemetry from nonhuman primatesMarc P Powell, William R Britz, James S Harper, et al.Pageof 105