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Journal of Medical Genetics|December 1, 1982
An autosomal dominant syndrome of uveal colobomata, cleft lip and palate, and mental retardationH M Kingston, P S Harper, P W JonesDevelopmental Medicine and Child Neurology|June 1, 1990
Early development of boys with Duchenne muscular dystrophyR A Smith, J R Sibert, P S HarperBiochimica Et Biophysica Acta|November 9, 1982
Multiple forms of iduronate 2-sulphate sulphatase in human tissues and body fluidsI M Archer, P S Harper, F S WustemanQJM : Monthly Journal of the Association of Physicians|November 1, 1994
Motor neurone disease--a study of prevalence and disabilityC M James, P S Harper, C M WilesPrenatal Diagnosis|May 1, 1984
Prenatal diagnosis of Hunter syndromeI M Archer, H M Kingston, P S HarperJournal 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 CompstonPageof 23