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Lancet (London, England)|September 9, 1989
Problems in genetic prediction for Huntington's diseaseM J Morris, A Tyler, L Lazarou, et al.Journal of Medical Genetics|December 1, 1989
Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markersA M Norman, J L Floyd, A L Meredith, et al.Journal of Medical Genetics|August 1, 1989
Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of WalesL A Tyfield, A L Meredith, M J Osborn, et al.Archives of Disease in Childhood|July 1, 1979
Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated casesJ R Sibert, P S Harper, R J Thompson, et al.Journal of Medical Genetics|April 1, 1990
Becker muscular dystrophy: correlation of deletion type with clinical severityA M Norman, N S Thomas, H M Kingston, et al.Clinical Genetics|January 1, 1995
Risk estimates for developing motor neurone disease in first-degree relativesC M James, R G Newcombe, P S Harper, et al.Archives of Disease in Childhood|June 1, 1989
Early diagnosis and secondary prevention of Duchenne muscular dystrophyR A Smith, J R Sibert, S J Wallace, et al.American Journal of Medical Genetics|June 19, 1995
Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection libraryM Upadhyaya, M Osborn, J Maynard, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1996
Neuropathological diagnosis and CAG repeat expansion in Huntington's diseaseJ H Xuereb, J C MacMillan, R Snell, et al.Clinical Genetics|December 1, 1990
Attitudes of parents of cystic fibrosis children towards neonatal screening and antenatal diagnosisL N al-Jader, M C Goodchild, H C Ryley, et al.Pageof 23