D.E. Wilcox

Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity

Fernando Morales, Jillian M. Couto, Catherine F. Higham et al. · Human Molecular Genetics · 2012 · 179 citations · Full text

Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study

Anthonie J. van Essen, Stephen Abbs, Montserrat Baiget et al. · Human Genetics · 1992 · 98 citations

Developmental Biology, Dystrophin Gene, Genetic Disorder +8

Life expectancy and death from cardiomyopathy amongst carriers of Duchenne and Becker muscular dystrophy in Scotland

S Holloway, D.E. Wilcox, Allen J. Wilcox et al. · Heart · 2007 · 47 citations

Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry

D.E. Wilcox, Alexander Cooke, J. Coigan et al. · Human Genetics · 1986 · 38 citations

Flow Cytometry, Mendelian Disorder, Genetic Disorder +8

Modafinil for excessive daytime sleepiness in myotonic dystrophy type 1 – The patients’ perspective

David Hilton‐Jones, M. Bowler, H. Lochmueller et al. · Neuromuscular Disorders · 2012 · 37 citations

Sleep Disorders, Sleep, Sleep Medicine +5