An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference29 articles.
1. A strategy to reveal high frequency RFLP's along the human X chromosome;Aldridge;Amer. J. Hum. Genet,1984
2. Screening lambdagt recombinant clones by hybridization to single plaques in situ;Benton;Science,1977
3. Construction and characteristics of new cloning vehicles. II. A multipurpose cloning system;Bolivar;Gene,1977
4. Organization and expression of eukaryotic split genes coding for proteins;Breathnach;Annu. Rev. Biochem,1981
5. A cDNA clone from the Duchenne/Becker muscular dystrophy gene;Burghes;Nature (London),1987
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