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Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy

โœ Scribed by Ray, Peter N.; Belfall, Bonnie; Duff, Catherine; Logan, Cairine; Kean, Vanora; Thompson, Margaret W.; Sylvester, James E.; Gorski, Jerome L.; Schmickel, Roy D.; Worton, Ronald G.


Book ID
109742201
Publisher
Nature Publishing Group
Year
1985
Tongue
English
Weight
501 KB
Volume
318
Category
Article
ISSN
0028-0836

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Mapping of X chromosome translocation br
โœ D. J. Cockburn; E. A. Munro; I. W. Craig; Y. Boyd ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Springer ๐ŸŒ English โš– 690 KB

There are rare female patients who suffer from Duchenne or Becker muscular dystrophy because they carry an X;autosome translocation with a breakpoint in the dystrophin gene. We have defined the positions of seven of these breakpoints with respect to exon-containing HindIII fragments detected by dyst