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D E Barton

Showing results (21-30 of 65) with videos related to

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Human Molecular Genetics|November 1, 1994
Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populationsD C Rubinsztein, J Leggo, W Amos, et al.
American Journal of Medical Genetics|April 24, 1995
Normal CAG and CCG repeats in the Huntington's disease genes of Parkinson's disease patientsD C Rubinsztein, J Leggo, S Goodburn, et al.
Thorax|January 1, 1997
Cystic fibrosis diagnosed by molecular genetic investigation in the mother of a patient with cystic fibrosisG A Gregory, D A Woolf, R McMahon, et al.
Genomics|April 1, 1993
Genetic mapping of X-linked ocular albinism: linkage analysis in a large Newfoundland kindredS J Charles, J S Green, A T Moore, et al.
Genomics|July 1, 1989
Mapping of genes for inhibin subunits alpha, beta A, and beta B on human and mouse chromosomes and studies of jsd miceD E Barton, T L Yang-Feng, A J Mason, et al.
Journal of Medical Genetics|November 14, 1997
Instability of normal (CTG)n alleles in the DM kinase geneD J Dow, D C Rubinsztein, J R Yates, et al.
Nucleic Acids Research|December 23, 1987
The human U1-70K snRNP protein: cDNA cloning, chromosomal localization, expression, alternative splicing and RNA-bindingR A Spritz, K Strunk, C S Surowy, et al.
The British Journal of Ophthalmology|July 1, 1994
Carrier detection in X linked ocular albinism using linked DNA polymorphismsS J Charles, A T Moore, Y Zhang, et al.
Genomics|September 1, 1987
Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: functional locus identified by its amplification in hydroxyurea-resistant cell linesT L Yang-Feng, D E Barton, L Thelander, et al.
Development (Cambridge, England)|May 1, 1990
Molecular analysis of the Mov 34 mutation: transcript disrupted by proviral integration in mice is conserved in DrosophilaT Gridley, D A Gray, T Orr-Weaver, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|November 1, 1994
Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populationsD C Rubinsztein, J Leggo, W Amos, et al.
American Journal of Medical Genetics|April 24, 1995
Normal CAG and CCG repeats in the Huntington's disease genes of Parkinson's disease patientsD C Rubinsztein, J Leggo, S Goodburn, et al.
Thorax|January 1, 1997
Cystic fibrosis diagnosed by molecular genetic investigation in the mother of a patient with cystic fibrosisG A Gregory, D A Woolf, R McMahon, et al.
Genomics|April 1, 1993
Genetic mapping of X-linked ocular albinism: linkage analysis in a large Newfoundland kindredS J Charles, J S Green, A T Moore, et al.
Genomics|July 1, 1989
Mapping of genes for inhibin subunits alpha, beta A, and beta B on human and mouse chromosomes and studies of jsd miceD E Barton, T L Yang-Feng, A J Mason, et al.
Journal of Medical Genetics|November 14, 1997
Instability of normal (CTG)n alleles in the DM kinase geneD J Dow, D C Rubinsztein, J R Yates, et al.
Nucleic Acids Research|December 23, 1987
The human U1-70K snRNP protein: cDNA cloning, chromosomal localization, expression, alternative splicing and RNA-bindingR A Spritz, K Strunk, C S Surowy, et al.
The British Journal of Ophthalmology|July 1, 1994
Carrier detection in X linked ocular albinism using linked DNA polymorphismsS J Charles, A T Moore, Y Zhang, et al.
Genomics|September 1, 1987
Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: functional locus identified by its amplification in hydroxyurea-resistant cell linesT L Yang-Feng, D E Barton, L Thelander, et al.
Development (Cambridge, England)|May 1, 1990
Molecular analysis of the Mov 34 mutation: transcript disrupted by proviral integration in mice is conserved in DrosophilaT Gridley, D A Gray, T Orr-Weaver, et al.
Pageof 7