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Journal of Medical Genetics|September 1, 1991
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17M C Koch, K Ricker, M Otto, et al.Human Genetics|November 1, 1991
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17M C Koch, K Ricker, M Otto, et al.Journal of Medical Genetics|December 1, 1985
Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales familiesP S Harper, S Youngman, M A Anderson, et al.Nature|February 6, 1992
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophyH G Harley, J D Brook, S A Rundle, et al.Human Genetics|May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19qH G Harley, K V Walsh, S Rundle, et al.Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.Human Genetics|January 1, 1985
Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophyC S Brown, N S Thomas, M Sarfarazi, et al.American Journal of Human Genetics|July 1, 1991
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA markerH G Harley, J D Brook, J Floyd, et al.Genomics|November 1, 1988
Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locusH G Harley, J D Brook, C L Jackson, et al.Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.Pageof 23