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Mutation Research|June 6, 2000
Individual variation in somatic mutations of the glycophorin-A gene in neonates in relation to pre-natal factorsC P Daniel, A Fisher, L Parker, et al.Journal of Medical Genetics|March 1, 1995
Kabuki syndrome-like features in monozygotic twin boys with a pseudodicentric chromosome 13S A Lynch, K A Ashcroft, S Zwolinski, et al.Clinical Genetics|May 1, 1992
Lethal congenital erythroderma: a newly recognised genetic disorderJ P Shield, M R Judge, W Reardon, et al.Annals of Neurology|May 13, 1999
The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twinsP Piccini, D J Burn, R Ceravolo, et al.Journal of Chromatography. A|June 16, 2001
Experimental studies of uncertainties associated with chromatographic techniquesV J Barwick, S L Ellison, C L Lucking, et al.Stroke|February 1, 1994
Long-term risk of recurrent stroke after a first-ever stroke. The Oxfordshire Community Stroke ProjectJ Burn, M Dennis, J Bamford, et al.Journal of the American Geriatrics Society|September 27, 2005
Prevalence and severity of gait disorders in Alzheimer's and non-Alzheimer's dementiasLouise M Allan, Clive G Ballard, David J Burn, et al.International Journal of Geriatric Psychiatry|July 22, 2005
Longitudinal study of cerebral blood flow SPECT in Parkinson's disease with dementia, and dementia with Lewy bodiesMichael J Firbank, David J Burn, Ian G McKeith, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 24, 2005
Brain atrophy rates in Parkinson's disease with and without dementia using serial magnetic resonance imagingEmma J Burton, Ian G McKeith, David J Burn, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|January 1, 1997
Strategies for antenatal detection of Down's syndromeJ P Wyllie, R J Madar, M Wright, et al.Pageof 60