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S A Rundle

Showing results (11-20 of 21) with videos related to

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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.
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.
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.
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.
Genomics|June 1, 1992
Radiation-reduced hybrids for the myotonic dystrophy locusJ D Brook, B V Zemelman, K Hadingham, 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.
Cytogenetics and Cell Genetics|January 1, 1992
Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19A Mitchell, A E Bale, B J Lee, et al.
Human Genetics|May 1, 1991
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessmentsJ D Brook, S J Knight, S H Roberts, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
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.
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.
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.
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.
Genomics|June 1, 1992
Radiation-reduced hybrids for the myotonic dystrophy locusJ D Brook, B V Zemelman, K Hadingham, 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.
Cytogenetics and Cell Genetics|January 1, 1992
Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19A Mitchell, A E Bale, B J Lee, et al.
Human Genetics|May 1, 1991
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessmentsJ D Brook, S J Knight, S H Roberts, et al.
Pageof 3