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Journal of Medical Genetics|September 1, 1992
Mutation analysis of 184 cystic fibrosis families in WalesJ Cheadle, J Myring, L al-Jader, et al.The British Journal of Psychiatry : the Journal of Mental Science|October 1, 1992
Presymptomatic testing for Huntington's disease in Wales 1987-90A Tyler, M Morris, L Lazarou, et al.Journal of Microscopy|February 1, 1988
Soft X-ray contact imaging of nucleolar chromatin using synchrotron radiation: a comparative scanning and transmission electron microscope studyR S Hill, W J Myring, D T Clarke, 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.Journal of Medical Genetics|November 1, 1992
Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophyJ Myring, A L Meredith, H G Harley, et al.Human Molecular Genetics|September 25, 1997
The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosisM M Maheshwar, J P Cheadle, A C Jones, et al.Lancet (London, England)|May 9, 1992
Unstable DNA sequence in myotonic dystrophyH G Harley, S A Rundle, W Reardon, et al.The British Journal of Ophthalmology|September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosisW Reardon, J C MacMillan, J Myring, et al.Neuromuscular Disorders : NMD|November 26, 1998
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafnessM F Phillips, M T Rogers, R Barnetson, et al.Pageof 2