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Journal of Medical Genetics|November 1, 1989
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counsellingS M Huson, D A Compston, P S HarperJournal of Medical Genetics|September 1, 1987
Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markersM Upadhyaya, M Sarfarazi, S M Huson, et al.Journal of Medical Genetics|November 1, 1996
Huntington's disease predictive testing: the case for an assessment approach to requests from adolescentsJ Binedell, J R Soldan, J Scourfield, et al.Archives of Disease in Childhood|October 1, 1987
Clinical aspects of X-linked hypohidrotic ectodermal dysplasiaA Clarke, D I Phillips, R Brown, et al.Journal of Medical Genetics|May 1, 1989
Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long armS H Roberts, M Upadhyaya, M Sarfarazi, et al.Journal of Medical Genetics|March 1, 1988
Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8)O W Quarrell, S Youngman, M Sarfarazi, et al.Clinical Genetics|November 1, 1986
The problem of isolated cases of Huntington's disease in South Wales 1974-1984O W Quarrell, A Tyler, G Cole, et al.American Journal of Medical Genetics|December 1, 1987
An integrated microcomputer system to maintain a genetic register for Huntington diseaseM Sarfarazi, O W Quarrell, G Wolak, et al.Journal of Medical Genetics|September 1, 1989
Duchenne muscular dystrophy in Wales: a 15 year study, 1971 to 1986A M Norman, C Rogers, J R Sibert, et al.Archives of Disease in Childhood|March 1, 1986
The use of flanking markers in prediction for Duchenne muscular dystrophyH Williams, M Sarfarazi, C Brown, et al.Pageof 23