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Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
The pathogenesis of multiple system atrophy: past, present, and futureE Jaros, D J BurnJournal of Medical Genetics|May 1, 1990
Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitaliaM E Porteous, J BurnBiology of the Neonate|January 1, 1976
Isoelectric focusing of non-specific esterases of developing human brain in thin-layer polyacrylamide gelsS S Papiha, J BurnJournal of Neurology, Neurosurgery, and Psychiatry|July 1, 1981
Biochemical and clinical studies of Friedreich's ataxiaP Purkiss, M Baraitser, O Borud, et al.Clinical Genetics|September 1, 1990
Frontonasal dysplasia or craniofrontonasal dysplasia and the Poland anomaly?W Reardon, I K Temple, B Jones, et al.Neuropediatrics|November 1, 1987
The use of a computerised database for the diagnosis of a rare neurological syndromeK Tomiwa, M Baraitser, E M Brett, et al.Molecular Pathology : MP|November 29, 2001
Multiple system atrophy: cellular and molecular pathologyD J Burn, E JarosCytogenetics and Cell Genetics|November 5, 1999
Genetic predictive testing for bowel cancer predisposition: the impact on the individualP D Chapman, J BurnIntensive Care Medicine|July 1, 1978
The effects of insulin glucose administration in fulminant hepatic failureJ Burn, W D WilliamsClinical Genetics|March 1, 1991
Atypical facio-scapulo-humeral muscular dystrophy--a counselling dilemmaW Reardon, I K Temple, G Harwood, et al.Pageof 60