1. Duchenne muscular dystrophy: high frequency of deletions;Bartlett, R.J.; Pericak-Vance, M.A.; Koh, J.;Neurology,1988
2. Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy;Speer, M.C.; Pericak-Vance, M.A.; Yamaoka, L.H.;Prenat Diagn,1988
3. Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometry;Laing, N.G.; Siddique, T.; Bartlett, R.;Clin Genet,1989
4. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization 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
5. Topography of the Duchenne muscular dystrophy gene: FIGE and cDNA analysis of;JT, Den Dunnen; PM, Grootscholten; E, Bakker;Am J Hum Genet; cases reveals 115 deletions and 13 duplications,1989