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H G Harley

Showing results (11-20 of 35) with videos related to

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Journal of Medical Genetics|November 1, 1992
Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophyJ Myring, A L Meredith, H G Harley, et al.
Journal of Medical Genetics|March 1, 1993
A study of DNA methylation in myotonic dystrophyD J Shaw, S Chaudhary, S A Rundle, et al.
Nucleic Acids Research|February 25, 1990
A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245)J D Brook, M Upadhyaya, W Broadhead, 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.
The British Journal of Ophthalmology|September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosisW Reardon, J C MacMillan, J Myring, et al.
Clinical Genetics|April 1, 1993
The DM mutation; diagnostic applications in the Finnish populationP Nokelainen, P Shelbourne, D Shaw, et al.
Neuromuscular Disorders : NMD|November 26, 1998
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafnessM F Phillips, M T Rogers, R Barnetson, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|November 1, 1992
Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophyJ Myring, A L Meredith, H G Harley, et al.
Journal of Medical Genetics|March 1, 1993
A study of DNA methylation in myotonic dystrophyD J Shaw, S Chaudhary, S A Rundle, et al.
Nucleic Acids Research|February 25, 1990
A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245)J D Brook, M Upadhyaya, W Broadhead, 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.
The British Journal of Ophthalmology|September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosisW Reardon, J C MacMillan, J Myring, et al.
Clinical Genetics|April 1, 1993
The DM mutation; diagnostic applications in the Finnish populationP Nokelainen, P Shelbourne, D Shaw, et al.
Neuromuscular Disorders : NMD|November 26, 1998
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafnessM F Phillips, M T Rogers, R Barnetson, et al.
Pageof 4