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Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophy in cDNA |
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| Authors: | Basil T. Darras Michel Koenig Louis M. Kunkel Uta Francke John M. Optiz James F. Reynolds |
| Abstract: | |
| Keywords: | Duchenne muscular dystrophy dystrophin cDNA prenatal diagnosis restriction fragment length polvmorphisms X chromosome |