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J C Macmillan

Showing results (21-30 of 34) with videos related to

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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.
Cephalalgia : an International Journal of Headache|September 4, 2010
Association of a Notch 3 gene polymorphism with migraine susceptibilityS Menon, H C Cox, M Kuwahata, 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.
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.
Human Genetics|May 1, 1993
Charcot-Marie-tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2-->12M Upadhyaya, S H Roberts, J Farnham, et al.
Brain Research|January 4, 2011
Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraineS Menon, J Buteri, B Roy, et al.
Immunological Investigations|June 1, 2005
Serum TGF-beta 1 and TNF-alpha levels and cardiac fibrosis in experimental chronic renal failureAlexey V Fedulov, T P Ses, N A Gavrisheva, et al.
Nature Genetics|September 10, 1998
PAK3 mutation in nonsyndromic X-linked mental retardationK M Allen, J G Gleeson, S Bagrodia, et al.
Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.
American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
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.
Cephalalgia : an International Journal of Headache|September 4, 2010
Association of a Notch 3 gene polymorphism with migraine susceptibilityS Menon, H C Cox, M Kuwahata, 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.
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.
Human Genetics|May 1, 1993
Charcot-Marie-tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2-->12M Upadhyaya, S H Roberts, J Farnham, et al.
Brain Research|January 4, 2011
Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraineS Menon, J Buteri, B Roy, et al.
Immunological Investigations|June 1, 2005
Serum TGF-beta 1 and TNF-alpha levels and cardiac fibrosis in experimental chronic renal failureAlexey V Fedulov, T P Ses, N A Gavrisheva, et al.
Nature Genetics|September 10, 1998
PAK3 mutation in nonsyndromic X-linked mental retardationK M Allen, J G Gleeson, S Bagrodia, et al.
Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.
American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
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