Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysisAndrew Read, J. L. H. O’Riordan, Roger Smith et al.|Human Genetics|1986Cited by 81
Bridging markers defining the map position of X linked hypophosphataemic rickets.Rajesh V. Thakker, Andrew King, Andrew Read et al.|Journal of Medical Genetics|1987Cited by 56
Patterns of exon deletions in Duchenne and Becker muscular dystrophyAndrew Read, R Harris, R. Mountford et al.|Human Genetics|1988Cited by 41
A register based system for gene tracking in Duchenne muscular dystrophy.Andrew Read, R Harris, L Kerzin-Storrar et al.|Journal of Medical Genetics|1986Cited by 21
DNA PROBES IN DIFFERENTIAL DIAGNOSIS OF BECKER MUSCULAR DYSTROPHY AND SPINAL MUSCULAR ATROPHYPeter Lunt, R Harris, W. J. K. Cumming et al.|The Lancet|1989Cited by 19