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Journal of Medical Genetics|March 1, 1993
A study of DNA methylation in myotonic dystrophyD J Shaw, S Chaudhary, S A Rundle, 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.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.Lancet (London, England)|May 9, 1992
Unstable DNA sequence in myotonic dystrophyH G Harley, S A Rundle, W Reardon, et al.Journal of Medical Genetics|February 1, 1991
Identification of new DNA markers close to the myotonic dystrophy locusJ D Brook, H G Harley, K V Walsh, et al.Human Genetics|August 1, 1989
Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sitesD J Shaw, H G Harley, J D Brook, 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.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.American Journal of Human Genetics|June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophyH G Harley, S A Rundle, J C MacMillan, et al.Genomics|December 1, 1993
Genomic organization and transcriptional units at the myotonic dystrophy locusD J Shaw, M McCurrach, S A Rundle, et al.Pageof 21