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Journal of Medical Genetics|March 1, 1993
A study of DNA methylation in myotonic dystrophyD J Shaw, S Chaudhary, S A Rundle, et al.Human Genetics|January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locusD J Shaw, A L Meredith, M Sarfarazi, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2006
A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?A J Murray, T A T Hughes, J W Neal, et al.Journal of Medical Genetics|November 1, 1992
Minimal expression of myotonic dystrophy: a clinical and molecular analysisW Reardon, H G Harley, J D Brook, et al.Clinical Genetics|March 1, 1993
Huntington's disease: predictive testing and the molecular genetics laboratoryL P Lazarou, A L Meredith, J M Myring, et al.British Medical Journal (Clinical Research Ed.)|May 12, 1984
Contribution of isolated general practitioner maternity unitsA J Cavenagh, K M Phillips, B Sheridan, et al.British Medical Journal|January 10, 1976
Climate and painful crisis of sickle-cell disease in JamaicaA M Redwood, E M Williams, P Desal, et al.Journal of Clinical Monitoring and Computing|February 13, 2003
An IBM PC-based system for the assessment of cardio-respiratory function using oscillating inert gas forcing signalsL S Wong, E M Williams, R Hamilton, et al.Respiration Physiology|April 1, 1997
A reconciliation of continuous and tidal ventilation gas exchange modelsM C Sainsbury, A Lorenzi, E M Williams, et al.Physiological Measurement|October 27, 2011
Estimation of tidal ventilation in preterm and term newborn infants using electromagnetic inductance plethysmographyE M Williams, N Pickerd, M Eriksen, et al.Pageof 30