
doi: 10.1007/bf00319691
pmid: 4120886
Mouse chromosomes banded by quinacrine mustard staining, by the ASG technique, or by Giemsa staining following trypsinization or chymotrypsinization are described in detail. Three hundred and twelve regions within the mouse karyotype can be distinguished and a simple system of nomenclature is proposed for naming these regions. This nomenclature is applied to discussion of the locations of the breakpoints of twenty translocations and of many specific gene loci.
Chromosome Aberrations, C3H/HE, DBA/1 (12), Staining and Labeling, Genes:, C57BL/6, Chromosome Mapping, NZB, Chromosomes, Cytogenetics, Mice, Genes, Quinacrine, Karyotyping, Terminology as Topic, Cellular Biology:, Animals, Chymotrypsin, Trypsin, Strains: A(CAL-A) (A/J), BALB/C, CBA
Chromosome Aberrations, C3H/HE, DBA/1 (12), Staining and Labeling, Genes:, C57BL/6, Chromosome Mapping, NZB, Chromosomes, Cytogenetics, Mice, Genes, Quinacrine, Karyotyping, Terminology as Topic, Cellular Biology:, Animals, Chymotrypsin, Trypsin, Strains: A(CAL-A) (A/J), BALB/C, CBA
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 489 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 0.1% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |
