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P S Harper

Showing results (191-200 of 216) with videos related to

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Human Molecular Genetics|July 1, 1993
Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangementsM Upadhyaya, P Jardine, J Maynard, et al.
Human Genetics|November 1, 1986
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19D J Shaw, A L Meredith, J D Brook, et al.
Clinical Genetics|March 1, 1997
Carrier screening for cystic fibrosis in primary care: evaluation of a project in South Wales. The South Wales Cystic Fibrosis Carrier Screening Research TeamY Payne, M Williams, J Cheadle, et al.
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.
Pageof 22

Showing results (191-200 of 216) with videos related to

Sort By:
Pageof 22
Human Molecular Genetics|July 1, 1993
Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangementsM Upadhyaya, P Jardine, J Maynard, et al.
Human Genetics|November 1, 1986
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19D J Shaw, A L Meredith, J D Brook, et al.
Clinical Genetics|March 1, 1997
Carrier screening for cystic fibrosis in primary care: evaluation of a project in South Wales. The South Wales Cystic Fibrosis Carrier Screening Research TeamY Payne, M Williams, J Cheadle, et al.
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.
Pageof 22