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Clinical features in a girl with Duchenne muscular dystrophy with an X-autosome translocation; (X;4)(p21;q26)

✍ Scribed by Kimura, Seiji; Mitsuda, Toshiro; Misugi, Nobuko; Saito, Fumiko; Tonomura, Akira; Sugita, Hideo

Book ID
123474688
Publisher
Elsevier Science
Year
1986
Tongue
English
Weight
652 KB
Volume
8
Category
Article
ISSN
0387-7604

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✍ D. J. Cockburn; E. A. Munro; I. W. Craig; Y. Boyd πŸ“‚ Article πŸ“… 1992 πŸ› Springer 🌐 English βš– 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