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Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1995
Molecular diagnostic analysis for Huntington's disease: a prospective evaluationJ C MacMillan, P Davies, P S HarperJournal 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|October 1, 1992
The Charcot-Marie-Tooth syndrome: perceptions of disability and projected use of DNA diagnostic testsJ C MacMillan, P S HarperAnnals of Neurology|September 1, 1991
Single-gene neurological disorders in South Wales: an epidemiological studyJ C MacMillan, P S HarperClinical Genetics|March 1, 1994
The Charcot-Marie-Tooth syndrome: clinical aspects from a population study in South Wales, UKJ C MacMillan, P S HarperJournal of Medical Genetics|January 1, 1992
Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales familiesJ C MacMillan, M Upadhyaya, P S HarperHuman Molecular Genetics|April 1, 1996
Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brainJ D Wood, J C MacMillan, P S Harper, 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.Nature Genetics|August 1, 1993
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's diseaseR G Snell, J C MacMillan, J P Cheadle, et al.Experimental Neurology|May 30, 1998
Huntingtin protein colocalizes with lesions of neurodegenerative diseases: An investigation in Huntington's, Alzheimer's, and Pick's diseasesS K Singhrao, P Thomas, J D Wood, et al.Pageof 142