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Lancet (London, England)|June 6, 1987
Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA markerO W Quarrell, A L Meredith, A Tyler, et al.Journal of Medical Genetics|August 1, 1983
The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophyP S Harper, T O'Brien, J M Murray, et al.Clinical Genetics|November 1, 1982
Mannosidosis in two brothers: prolonged survival in the severe phenotypeM A Patton, I C Barnes, I D Young, et al.Age and Ageing|November 1, 1994
Late-onset Huntington's disease: a clinical and molecular studyC M James, G D Houlihan, R G Snell, et al.Journal of Medical Genetics|August 1, 1983
Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequencesT O'Brien, P S Harper, K E Davies, et al.American Journal of Medical Genetics|January 1, 1990
Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysisJ Zonana, A Schinzel, M Upadhyaya, et al.American Journal of Respiratory and Critical Care Medicine|December 26, 2001
Changes in spirometry over time as a prognostic marker in patients with Duchenne muscular dystrophyM F Phillips, R C Quinlivan, R H Edwards, et al.Clinical Genetics|April 1, 1981
Huntington's Chorea in South Wales. A genetic and epidemiological studyD A Walker, P S Harper, C E Wells, et al.American Journal of Medical Genetics|August 1, 1992
Five years experience of predictive testing for myotonic dystrophy using linked DNA markersW Reardon, J L Floyd, J Myring, et al.Neuromuscular Disorders : NMD|January 1, 1992
Molecular analysis for the myotonic dystrophy mutation in neuromuscular disordersJ C MacMillan, J Myring, H G Harley, et al.Pageof 23