Approaches to determining mutation rates in human DNA
Identifieur interne : 004D57 ( Main/Exploration ); précédent : 004D56; suivant : 004D58Approaches to determining mutation rates in human DNA
Auteurs : John Delehanty [États-Unis] ; Raymond L. White [États-Unis] ; Mortimer L. Mendelsohn [États-Unis]Source :
- Mutation Research/Reviews in Genetic Toxicology [ 0165-1110 ] ; 1986.
English descriptors
- Teeft :
- Acad, Base change, Base changes, Base pairs, Caskey, Cell lines, Chromosome, Cohort, Considerable development, Cytogenetic, Cytogenetic methods, Deletion, Denaturing, Denaturing gradient, Determinant domain, Dos, Drosophila, Electromorphs, Endonuclease, Epidemiology, Fragment, Gene function, Genetic, Genetic disease, Genetic epidemiology, Genetic variation, Genome, Genomic, Genomic sequencing, Heritable, Heteroduplex, Heteroduplex analysis, Heteroduplexes, Hprt, Hprt gene, Human disease, Human genome, Human mutation, Human mutation rate, Human populations, Hybridization, Icpemc, Icpemc committee, Large number, Lerman, Locus, Mismatch, Molecular analysis, Mutagen, Mutant, Mutation, Mutation rate, Mutation rates, Natl, Neel, Nucleotide, Oligonucleotides, Phenotype, Point mutations, Polymorphism, Primary gradient, Probe, Proc, Rearrangement, Restriction enzymes, Rflp, Sentinel phenotypes, Sequencing, Somatic, Somatic cells, Somatic mutation, Specific gene probes, Substitution, Subtractive hybridization, Synthetic oligonucleotides.
Url:
DOI: 10.1016/0165-1110(86)90031-X
Affiliations:
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Mendelsohn</name><name sortKey="White, Raymond L" sort="White, Raymond L" uniqKey="White R" first="Raymond L." last="White">Raymond L. White</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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