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European Journal of Human Genetics : EJHG|January 1, 1996
Audit of maternal serum screening: strategies to augment counselling in response to women's viewsJ Burn, S Fairgrieve, P Franks, et al.American Journal of Human Genetics|July 1, 1994
A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individualsD Bourn, S A Carter, D G Evans, et al.Journal of Medical Genetics|November 1, 1987
Fetal valproate syndrome: is there a recognisable phenotype?R M Winter, D Donnai, J Burn, et al.International Journal of Colorectal Disease|March 1, 1993
The establishment of a polyposis registerS Bülow, J Burn, K Neale, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1990
A prospective study of acute cerebrovascular disease in the community: the Oxfordshire Community Stroke Project--1981-86. 2. Incidence, case fatality rates and overall outcome at one year of cerebral infarction, primary intracerebral and subarachnoid haemorrhageJ Bamford, P Sandercock, M Dennis, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 4, 2005
Characterizing behavioral and cognitive dysexecutive changes in progressive supranuclear palsyDavid Millar, Philipa Griffiths, Adam J Zermansky, et al.Physiological Measurement|April 11, 2006
Factors affecting the use of cumulative sums in the analysis of circadian blood pressureJ Burn, A J Sims, G A Ford, et al.Postgraduate Medical Journal|August 1, 1989
Strychnine poisoning as an unusual cause of convulsionsD J Burn, C R Tomson, J Seviour, et al.Human Genetics|March 1, 1994
Mutation screening by a combination of biotin-SSCP and direct sequencingA S Virdi, J A Loughlin, C M Irven, et al.Immunobiology|June 4, 2015
Patient stratification and therapy in atypical haemolytic uraemic syndrome (aHUS)Edwin Wong, Rachel Challis, Neil Sheerin, et al.Pageof 58