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The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome

โœ Scribed by Brockdorff, N.; Cross, G. S.; Cavanna, J. S.; Fisher, E. M. C.; Lyon, M. F.; Davies, K. E.; Brown, S. D. M.


Book ID
109749964
Publisher
Nature Publishing Group
Year
1987
Tongue
English
Weight
344 KB
Volume
328
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