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Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2003
Familial motor neurone disease with dementia: phenotypic variation and cerebellar pathologyT M Polvikoski, A Murray, P S Harper, et al.Journal of Medical Genetics|November 1, 1989
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severityS M Huson, D A Compston, P Clark, et al.Human Genetics|January 1, 1984
Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequencesH M Kingston, M Sarfarazi, N S Thomas, et al.American Journal of Human Genetics|July 1, 1992
Anticipation in myotonic dystrophy: new light on an old problemP S Harper, H G Harley, W Reardon, et al.Journal of Medical Genetics|February 1, 1983
Huntington's chorea in South Wales: mutation, fertility, and genetic fitnessD A Walker, P S Harper, R G Newcombe, et al.Archives of Disease in Childhood|February 1, 1993
The natural history of congenital myotonic dystrophy: mortality and long term clinical aspectsW Reardon, R Newcombe, I Fenton, et al.Journal of Public Health Medicine|June 1, 1993
Death certification by house officers and general practitioners--practice and performanceG Maudsley, E M WilliamsJournal of Public Health Medicine|March 1, 1996
"Inaccuracy' in death certification--where are we now?G Maudsley, E M WilliamsInternational Journal of Epidemiology|December 22, 1999
What lessons can be learned for cancer registration quality assurance from data users? Skin cancer as an exampleG Maudsley, E M WilliamsThe Journal of Physiology|June 1, 1981
The effect of prolonged propranolol administration on myocardial transmural capillary density in young rabbitsJ Tasgal, E M WilliamsPageof 30