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Genomics|January 1, 1993
Evidence for locus heterogeneity in autosomal dominant torsion dystoniaF Ahmad, M B Davis, H M Waddy, et al.Neurology|October 1, 1993
Genomic imprinting and anticipation in idiopathic torsion dystoniaM C LaBuda, N A Fletcher, A D Korczyn, et al.Archives of Disease in Childhood|October 15, 1998
Clinical and laboratory findings in referrals for mitochondrial DNA analysisP J Lamont, R Surtees, C E Woodward, et al.American Journal of Human Genetics|December 1, 1991
Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseasesJ Collinge, M Poulter, M B Davis, et al.Genomics|February 1, 1989
Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markersH R Middleton-Price, A E Harding, J Berciano, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1989
Tyrosine hydroxylase and levodopa responsive dystoniaN A Fletcher, I J Holt, A E Harding, et al.Lancet (London, England)|March 11, 1989
Molecular genetics of amyloid neuropathy in EuropeI J Holt, A E Harding, L Middleton, et al.Brain : a Journal of Neurology|June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic studyS R Hammans, M G Sweeney, M G Hanna, et al.Brain : a Journal of Neurology|April 1, 1995
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutationP Riordan-Eva, M D Sanders, G G Govan, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1982
X-linked recessive bulbospinal neuronopathy: a report of ten casesA E Harding, P K Thomas, M Baraitser, et al.Pageof 21