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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.American Journal of Human Genetics|June 1, 1991
Genetic risks for children of women with myotonic dystrophyM C Koch, T Grimm, H G Harley, et al.Journal of Medical Genetics|June 1, 1980
Ichthyosis, hepatosplenomegaly, and cerebellar degeneration in a sibshipP S Harper, R Marks, P J Dykes, et al.Journal of Genetic Counseling|July 5, 2015
Psychological Model for Presymptomatic Test Interviews: Lessons Learned from Huntington DiseaseJ Soldan, E Street, J Gray, et al.Journal of Medical Genetics|June 1, 1988
Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocationJ Zonana, S H Roberts, N S Thomas, et al.The British Journal of Psychiatry : the Journal of Mental Science|February 1, 1997
Huntington's disease: psychiatric practice in molecular genetic prediction and diagnosisJ Scourfield, J Soldan, J Gray, et al.Pageof 30