1. Review of studies on the proportion and origin of new mutants in Duchenne muscular dystrophy;Moser, H.,1984
2. Serum creatine kinase activity and carrier status for Duchenne muscular dystrophy;Bullock, D.G.; McSweeny, F.M.; Whitehead, T.P.; Edwards, J.H.;Lancet,1979
3. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X-chromosome;Davies, K.E.; Pearson, P.L.; Harper, P.S.;Nucleic Acids Res,1983
4. A strategy to reveal high frequency RFLPs along the human chromosome;Aldridge, J.; Kunkel, L.M.; Bruns, G.;Am J Hum Genet; Isolation of probes detecting RFLPs from X-chromosome specific libraries: potential use for diagnosis of Duchenne muscular dystrophy,1984
5. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs;Bakker, E.; Hofker, M.H.; Goor, N.;Lancet,1985