Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy
- 1 February 1992
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 42 (3) , 281-287
- https://doi.org/10.1002/ajmg.1320420304
Abstract
No abstract availableKeywords
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