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A L Meredith

Showing results (11-20 of 48) with videos related to

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Lancet (London, England)|August 9, 1986
First-trimester prediction in fetus at risk for myotonic dystrophyP W Lunt, A L Meredith, P S Harper
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 8, 1982
In vitro studies on calcium activated phosphatidylinositol phosphodiesterase of erythrocyte ghosts from normal individuals and those with myotonic muscular dystrophyA L Meredith, P S Harper, D M Bradley
Biotechnology & Genetic Engineering Reviews|January 1, 1985
Myotonic dystrophy and gene mapping on human chromosome 19J D Brook, D J Shaw, A L Meredith
Human Molecular Genetics|March 1, 1993
Two novel frame-shift mutations: 977 insA in exon 6B, and 4016 insT in exon 21, of the cystic fibrosis transmembrane conductance regulator (CFTR) geneJ P Cheadle, L N al-Jader, A L Meredith
Human Molecular Genetics|May 1, 1992
A new missense mutation (R1283M) in exon 20 of the cystic fibrosis transmembrane conductance regulator geneJ P Cheadle, A L Meredith, L N al-Jader
Human Molecular Genetics|July 1, 1993
A novel nonsense mutation, W846XI (amber termination), in exon 14a of the cystic fibrosis transmembrane conductance regulator (CFTR) geneJ P Cheadle, L N al-Jader, A L Meredith
Journal of Medical Genetics|August 1, 1992
Mild pulmonary disease in a cystic fibrosis child homozygous for R553XJ Cheadle, L al-Jader, M Goodchild, et al.
Journal of Medical Genetics|July 1, 1991
Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3S H Roberts, H E Hughes, S J Davies, et al.
Journal of Medical Genetics|February 1, 1995
Two CF patients, one homozygous for the 621 + 1G > T splice mutation, the other homozygous for the 1898 + 1G > A splice mutationJ P Cheadle, A L Meredith, L Millar-Jones, et al.
Journal of Medical Genetics|December 1, 1989
Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markersA M Norman, J L Floyd, A L Meredith, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Lancet (London, England)|August 9, 1986
First-trimester prediction in fetus at risk for myotonic dystrophyP W Lunt, A L Meredith, P S Harper
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 8, 1982
In vitro studies on calcium activated phosphatidylinositol phosphodiesterase of erythrocyte ghosts from normal individuals and those with myotonic muscular dystrophyA L Meredith, P S Harper, D M Bradley
Biotechnology & Genetic Engineering Reviews|January 1, 1985
Myotonic dystrophy and gene mapping on human chromosome 19J D Brook, D J Shaw, A L Meredith
Human Molecular Genetics|March 1, 1993
Two novel frame-shift mutations: 977 insA in exon 6B, and 4016 insT in exon 21, of the cystic fibrosis transmembrane conductance regulator (CFTR) geneJ P Cheadle, L N al-Jader, A L Meredith
Human Molecular Genetics|May 1, 1992
A new missense mutation (R1283M) in exon 20 of the cystic fibrosis transmembrane conductance regulator geneJ P Cheadle, A L Meredith, L N al-Jader
Human Molecular Genetics|July 1, 1993
A novel nonsense mutation, W846XI (amber termination), in exon 14a of the cystic fibrosis transmembrane conductance regulator (CFTR) geneJ P Cheadle, L N al-Jader, A L Meredith
Journal of Medical Genetics|August 1, 1992
Mild pulmonary disease in a cystic fibrosis child homozygous for R553XJ Cheadle, L al-Jader, M Goodchild, et al.
Journal of Medical Genetics|July 1, 1991
Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3S H Roberts, H E Hughes, S J Davies, et al.
Journal of Medical Genetics|February 1, 1995
Two CF patients, one homozygous for the 621 + 1G > T splice mutation, the other homozygous for the 1898 + 1G > A splice mutationJ P Cheadle, A L Meredith, L Millar-Jones, et al.
Journal of Medical Genetics|December 1, 1989
Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markersA M Norman, J L Floyd, A L Meredith, et al.
Pageof 5