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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
Huntington's disease: prediction and preventionP S Harper, O W Quarrell, S YoungmanClinical Genetics|January 23, 1999
Predictive testing for Huntington's disease: II. Qualitative findings from a study of uptake in South WalesJ Binedell, J R Soldan, P S HarperJournal of Clinical Pathology|October 1, 1985
Recombinant DNA studies on stored necropsy brain samples from patients with Huntington's choreaM Upadhyaya, G P Reynolds, P S HarperHuman Molecular Genetics|November 1, 1993
Neurofibromatosis type 1 (NF1): the search for mutations by PCR-heteroduplex analysis on Hydrolink gelsM H Shen, P S Harper, M UpadhyayaThe British Journal of Dermatology|May 1, 1979
A syndrome of ichthyosis, hepatosplenomegaly and cerebellar degenerationP J Dykes, R Marks, P S HarperJournal 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 HarperPageof 30