Showing results (1-10 of 234) with videos related to
Sort By:
Pageof 24
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 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 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 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.Human 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.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.Journal of Medical Genetics|December 1, 1993
Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary choreaJ C MacMillan, P J Morrison, N C Nevin, et al.Pageof 24