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L D McDaniel

Showing results (1-10 of 19) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15L D McDaniel, R A Schultz
Environmental and Molecular Mutagenesis|January 1, 1993
Elevation of sister chromatid exchange frequency in transformed human fibroblasts following exposure to widely used aminoglycosidesL D McDaniel, R A Schultz
Archives of Neurology|January 1, 1991
Anton's syndrome in a patient with posttraumatic optic neuropathy and bifrontal contusionsK D McDaniel, L D McDaniel
Journal of Geriatric Psychiatry and Neurology|October 1, 1993
Alzheimer's disease: the problem of incorrect clinical diagnosisL D McDaniel, T Lukovits, K D McDaniel
Marine Pollution Bulletin|June 25, 2015
Sand patties provide evidence for the presence of Deepwater Horizon oil on the beaches of the West Florida ShelfL D McDaniel, J Basso, E Pulster, et al.
Annales De Genetique|January 1, 1990
A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnanciesJ L Zackowski, L J Raffel, L D McDaniel, et al.
Somatic Cell and Molecular Genetics|April 18, 1998
Correction of the Bloom syndrome cellular phenotypesT Giesler, K Baker, B Zhang, et al.
Genes, Chromosomes & Cancer|November 1, 1992
Characterization of a complex chromosomal rearrangement maps the locus for in vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q13W L Flejter, L D McDaniel, M Askari, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair geneW L Flejter, L D McDaniel, D Johns, et al.
Human Mutation|January 1, 1997
Confirmation of homozygosity for a single nucleotide substitution mutation in a Cockayne syndrome patient using monoallelic mutation analysis in somatic cell hybridsL D McDaniel, R Legerski, A R Lehmann, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15L D McDaniel, R A Schultz
Environmental and Molecular Mutagenesis|January 1, 1993
Elevation of sister chromatid exchange frequency in transformed human fibroblasts following exposure to widely used aminoglycosidesL D McDaniel, R A Schultz
Archives of Neurology|January 1, 1991
Anton's syndrome in a patient with posttraumatic optic neuropathy and bifrontal contusionsK D McDaniel, L D McDaniel
Journal of Geriatric Psychiatry and Neurology|October 1, 1993
Alzheimer's disease: the problem of incorrect clinical diagnosisL D McDaniel, T Lukovits, K D McDaniel
Marine Pollution Bulletin|June 25, 2015
Sand patties provide evidence for the presence of Deepwater Horizon oil on the beaches of the West Florida ShelfL D McDaniel, J Basso, E Pulster, et al.
Annales De Genetique|January 1, 1990
A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnanciesJ L Zackowski, L J Raffel, L D McDaniel, et al.
Somatic Cell and Molecular Genetics|April 18, 1998
Correction of the Bloom syndrome cellular phenotypesT Giesler, K Baker, B Zhang, et al.
Genes, Chromosomes & Cancer|November 1, 1992
Characterization of a complex chromosomal rearrangement maps the locus for in vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q13W L Flejter, L D McDaniel, M Askari, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair geneW L Flejter, L D McDaniel, D Johns, et al.
Human Mutation|January 1, 1997
Confirmation of homozygosity for a single nucleotide substitution mutation in a Cockayne syndrome patient using monoallelic mutation analysis in somatic cell hybridsL D McDaniel, R Legerski, A R Lehmann, et al.
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