Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy. [electronic resource]

By: Contributor(s): Producer: 19920323Description: 281-7 p. digitalISSN:
  • 0148-7299
Subject(s): Online resources: In: American journal of medical genetics vol. 42
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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