Deletions in the 5' region of dystrophin and resulting phenotypes.

類似資料

• Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene.
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  出版事項: (1992)
• Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.
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  出版事項: (1993)
• Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion
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• A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart.
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• A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.
  著者:: Abbs, S, 等
  出版事項: (1991)