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Journal of Inherited Metabolic Disease|June 1, 1997
Huntington disease: advances in molecular and cell biologyA L Jones, J D Wood, P S HarperClinica Chimica Acta; International Journal of Clinical Chemistry|April 27, 1981
An improved assay for iduronate 2-sulphate sulphatase in serum and its use in the detection of carriers of the Hunter syndromeI M Archer, P S Harper, F S WustemanJournal of Medical Genetics|December 1, 1989
Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment biasP W Lunt, D A Compston, P S HarperClinica Chimica Acta; International Journal of Clinical Chemistry|April 8, 1982
In vitro studies on calcium activated phosphatidylinositol phosphodiesterase of erythrocyte ghosts from normal individuals and those with myotonic muscular dystrophyA L Meredith, P S Harper, D M BradleyBrain : a Journal of Neurology|December 1, 1988
Von Recklinghausen neurofibromatosis. A clinical and population study in south-east WalesS M Huson, P S Harper, D A CompstonJournal of Medical Genetics|November 1, 1989
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counsellingS M Huson, D A Compston, P S HarperJournal of Medical Genetics|September 1, 1987
Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markersM Upadhyaya, M Sarfarazi, S M Huson, et al.Journal of Medical Genetics|November 1, 1996
Huntington's disease predictive testing: the case for an assessment approach to requests from adolescentsJ Binedell, J R Soldan, J Scourfield, et al.Archives of Disease in Childhood|October 1, 1987
Clinical aspects of X-linked hypohidrotic ectodermal dysplasiaA Clarke, D I Phillips, R Brown, et al.Journal of Medical Genetics|May 1, 1989
Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long armS H Roberts, M Upadhyaya, M Sarfarazi, et al.Pageof 30