1. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organisation of the DMD gene in normal and affected individuals;Koenig, M.; Hoffman, E.P.; Bertelson, C.J.; Monaco, A.P.; Feener, C.; Kunkel, L.M.;Cell,1987
2. Preferential deletion of exons in Duchenne and Becker muscular dvstrophies;Forrest, S.M.; Cross, G.S.; Speer, A.; Gardner-Medwin, D.; Burn, J.; Davies, K.E.;Nature,1987
3. Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy;Hodgson, S.; Hart, K.; Abbs, S.;J Med Genet,1989
4. Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin and phenotype/ genotype correlation;Hu, X.; Ray, P.N.; Murphy, E.; Thompson, M.W.; Worton, R.G.;Am J Hum Genet,1989
5. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy;Hodgson, S.V.; Bobrow, M.;Br Med Bull,1989