1. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein;Koenig, M.; Monaco, A.P.; Kunkel, L.M.;Cell,1988
2. 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
3. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations;Darras, B.T.; Blattner, P.; Harper, J.F.; Spiro, A.J.; Alter, S.; Francke, U.;Am i Hum Genet,1988
4. Molecular deletion patterns in Duchenne and Becker type muscular dystrophy;Liechti-Gallati, S.; Koenig, M.; Kunkel, L.M.;Hum Genet,1989
5. Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy;Hofker, M.H.; Wapenaar, M.C.; Goor, N.; Bakker, E.; van Ommen, G.J.B.; Pearson, P.L.;Hum Genet,1985