Oocyte heterogeneity with respect to the meiotic silencing of unsynapsed X chromosomes in the XY female mouse

Mapping of X chromosome translocation br

Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene

✍ D. J. Cockburn; E. A. Munro; I. W. Craig; Y. Boyd 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 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