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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.Human Genetics|August 1, 1990
Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophyK V Walsh, H G Harley, J D Brook, et al.Journal of Medical Genetics|September 1, 1990
Genetic analysis of treated and untreated phenylketonuria in one familyL A Tyfield, A L Meredith, M J Osborn, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 20, 2002
Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weaknessM McEntagart, M Dunstan, C Bell, et al.Human Molecular Genetics|May 1, 1995
Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)P W Lunt, P E Jardine, M C Koch, et al.Experimental Neurology|May 30, 1998
Huntingtin protein colocalizes with lesions of neurodegenerative diseases: An investigation in Huntington's, Alzheimer's, and Pick's diseasesS K Singhrao, P Thomas, J D Wood, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|June 27, 1984
DNA and enzyme studies on chorionic villi for use in antenatal diagnosisM Upadhyaya, I M Archer, P S Harper, et al.Journal of Medical Genetics|November 1, 1989
Linkage disequilibrium in Huntington's disease: an improved localisation for the geneR G Snell, L P Lazarou, S Youngman, et al.Pageof 23