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Position of the translocation break T(2;9)138Ca in linkage group IX of the mouse

Published online by Cambridge University Press:  14 April 2009

Jan Klein  and
Dagmar Klein
Jan Klein
Affiliation:
Department of Oral Biology, School of Dentistry, and Department of Human Genetics, School of Medicine, The University of Michigan, Ann Arbor, Michigan 48104, U.S.A.
Dagmar Klein
Affiliation:
Department of Oral Biology, School of Dentistry, and Department of Human Genetics, School of Medicine, The University of Michigan, Ann Arbor, Michigan 48104, U.S.A.

Summary

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The translocation break T(2;9)138Ca is located about three map units from the H-2 region on the non-centromeric side of the IXth linkage group. The recombination frequency in the T-H-2 interval is increased in the presence of the T138 translocation to about twice its value in the absence of the translocation.

Type
Short Papers
Information
Genetics Research , Volume 19 , Issue 2 , April 1972 , pp. 177 - 179
Copyright
Copyright © Cambridge University Press 1972

References

REFERENCES

Boyse, E. A. & Old, L. J. (1969). Some aspects of normal and abnormal cell surface genetics. Annual Review of Genetics 3, 269–290.CrossRefGoogle Scholar
Carter, T. C., Lyon, M. F. & Phillips, R. J. S. (1955). Gene-tagged chromosome transloca-tions in eleven stocks of mice. Journal of Genetics 53, 154–166.CrossRefGoogle Scholar
Evans, E. P., Breckon, G. & Ford, C. E. (1964). An air-drying method for meiotic preparations from mammalian testes. Cytogenetics 3, 289–294.CrossRefGoogle ScholarPubMed
Gorer, P. A., Lyman, S. & Snell, G. D. (1948). Studies on the genetic and antigenetic basis of tumour transplantation. Linkage between a histocompatability gene and ‘fused’ in mice. Proceedings of the Royal Society B, 135, 499–505.Google Scholar
Green, M. C. (1966). Mutant genes and linkages. In Green, E. L. (ed.), Biology of the Laboratory Mouse, pp. 87–150. New York: McGraw-Hill.Google Scholar
Klein, J. (1971). Cytological identification of the chromosome carrying the IXth linkage group (including H-2) in the house mouse. Proceedings of the National Academy of Sciences, U.S.A. 68, 1594–1597.Google Scholar
Klein, J., Bednáâová, D. & Ŝrám, R. (1968). Crossing-over inside the H-2 locus accompanied by recombination of outside markers. Genetics 60, 241 (Abstract).Google Scholar
Klein, J., Klein, D. & Schreffler, D. C. (1970). H-2 types of translocation stocks T(2;9) 138Ca, T(9;13)190Ca and an H-2 recombinant. Transplantation 10, 309–320.CrossRefGoogle Scholar
Lyon, M. F. & Phillips, R. J. S. (1959). Crossing-over in mice heterozygous for t–alleles. Heredity 13, 23–32.CrossRefGoogle Scholar