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Lancet (London, England)|August 18, 1979
Huntington's chorea. The basis for long-term preventionP S Harper, D A Walker, A Tyler, et al.Journal of Medical Genetics|September 1, 1989
Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screeningA M Norman, M Upadhyaya, N S Thomas, et al.American Journal of Human Genetics|October 1, 1991
Covariate-dependent age-at-onset distributions for Huntington diseaseM Krawczak, B Bockel, L Sandkuijl, et al.Clinical Genetics|April 1, 1985
Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysisH M Kingston, M Sarfarazi, R G Newcombe, et al.Journal of the Neurological Sciences|December 1, 1988
Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14P W Lunt, J G Noades, M Upadhyaya, et al.Clinical Genetics|March 1, 1988
Population studies of Huntington's disease in WalesO W Quarrell, A Tyler, M P Jones, et al.Muscle & Nerve. Supplement|January 1, 1995
Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, J Maynard, M Osborn, et al.Muscle & Nerve. Supplement|April 12, 2013
Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, J Maynard, M Osborn, et al.Journal of Medical Genetics|August 1, 1987
Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales populationL P Lazarou, F Davies, M Sarfarazi, et al.American Journal of Human Genetics|August 1, 1992
The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, P Lunt, M Sarfarazi, et al.Pageof 23