1. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy;Murray, J.M.; Davies, K.E.; Harper, P.S.; Meredith, L.; Muller, C.R.; Williamson, R.;Nature,1982
2. Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa and McLeod syndrome;Francke, U.; Ochs, H.D.; de Martinville, B.;Am JHum Genet,1985
3. Isolation of candidate cDNAs for portions ofthe Duchenne muscular dystrophy gene;Monaco, A.P.; Neve, R.; Colletti-Feener, R.; Bertelson, C.J.; Kumit, M.; Kunkel, L.M.;Nature,1986
4. A cDNA clone from the Duchenne/Becker muscular dystrophin gene;Burghes, A.H.M.; Logan, C.; Hu, K.; Belfall, B.; Worton, R.G.; Ray, P.N.;Nature,1987
5. Complete cloning of the Duchenne muscular dystrophy DMD cDNA and preliminary genomic organization of the DMD gene in formal and affected individuals;Koenig, M.; Hoffmann, E.; Bertelson, C.J.; Monaco, A.; Feener, C.; Kunkel, L.M.;Cell,1987