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Heart (British Cardiac Society)|April 1, 1997
Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxyM Penman Splitt, M Y Tsai, J Burn, et al.Age and Ageing|August 22, 2012
New horizons in the pathogenesis, assessment and management of movement disordersGordon W Duncan, Alison J Yarnall, Sarah Marrinan, et al.Journal of Medical Genetics|May 1, 1987
Angelman (happy puppet) syndrome in a girl and her brotherJ A Fisher, J Burn, F W Alexander, et al.Australian Veterinary Journal|December 24, 1997
Experimental Leptospira borgpetersenii serovar hardjo infection of pregnant cattleC R Smith, M R McGowan, C S McClintock, et al.Annals of Human Genetics|May 1, 1982
Mapping studies on human mitochondrial glutamate oxaloacetate transaminaseS J Jeremiah, S Povey, M W Burley, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 21, 2006
The basal ganglia cholinergic neurochemistry of progressive supranuclear palsy and other neurodegenerative diseasesN M Warren, M A Piggott, A J Lees, et al.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.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.Pageof 49