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A genetic mapping procedure, called the duplication-deficiency method, is described. This method permits the genetic location of a translocation to be determined within a linkage group without the use of recombination. By utilizing the duplication-deficiency method to define the genetic breakpoints for a series of translocations involving a given chromosome and integrating this information with their cytological breakpoints, obtained by Giemsa banding, a genetic map of the chromosomes is constructed whereby groups of loci are assigned to banded regions. Duplication-deficiency mapping and Giemsa banding analysis of the T(X;7)1Ct and T(7;19)145H translocations together with information from the c25H deletion have permitted mouse chromosome 7 to be divided into six and chromosome 19 into two definable genetic regions.
E M Eicher, and
L L Washburn
April 1994,
Mammalian genome : official journal of the International Mammalian Genome Society,
E M Eicher, and
L L Washburn
January 1989,
Progress in clinical and biological research,
E M Eicher, and
L L Washburn
October 1986,
Proceedings of the National Academy of Sciences of the United States of America,
E M Eicher, and
L L Washburn
February 1986,
Journal of interferon research,
E M Eicher, and
L L Washburn
December 1993,
Genomics,
E M Eicher, and
L L Washburn
January 1984,
Proceedings of the National Academy of Sciences of the United States of America,
E M Eicher, and
L L Washburn
September 1978,
Proceedings of the National Academy of Sciences of the United States of America,
E M Eicher, and
L L Washburn
June 1995,
FEMS microbiology letters,
E M Eicher, and
L L Washburn
January 1973,
Birth defects original article series,
E M Eicher, and
L L Washburn
January 2006,
Cytogenetic and genome research,
