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2. Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy;Gillard, E.F.; Chamberlain, J.S.; Murphy, E.G.;(DMD) gene. Am 7 Hum Genet,1989
3. Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin and phenotype/genotype correlation;Hu, X.; Ray, P.N.; Murphy, E.G.; Thompson, M.W.; Worton, R.G.;Am J Hum Genet,1990
4. Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations;Roberts, R.G.; Gardner, R.J.; Bobrow, M.;Hum Mutat,1994
5. Point mutation in a Becker muscular dystrophy patient;Roberts, R.G.; Passos-Bueno, M.R.; Bobrow, M.; Vainzof, M.; Zatz, M.;Hum Mol Genet,1992