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J C MacMillan

Showing results (21-30 of 45) with videos related to

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The British Journal of Radiology|June 1, 1986
Technetium-99m Medronate uptake in subcutaneous soft-tissue nodules in a patient with renal failure and renal adenocarcinomaJ C MacMillan, S J Scott, M I McHugh, et al.
Journal of Telemedicine and Telecare|December 19, 2001
Telemedicine and clinical genetics: establishing a successful serviceM R Gattas, J C MacMillan, I Meinecke, et al.
Journal 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.
Annals of Surgical Oncology|October 13, 2001
Comparative expression of the mitotic regulators SAK and PLK in colorectal cancerJ C Macmillan, J W Hudson, S Bull, 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.
The Journal of Thoracic and Cardiovascular Surgery|February 1, 1978
Internal configuration of saphenous-coronary anastomoses as studied by the cast-injection techniqueJ N Young, J C MacMillan, I A May, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|September 30, 2005
A population genomics overview of the neuronal nitric oxide synthase (nNOS) gene and its relationship to migraine susceptibilityM P Johnson, R A Lea, N J Colson, 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.
Biochemical Society Transactions|November 1, 1995
Characterising the Huntington's disease gene productJ Wood, J C MacMillan, P Thomas, et al.
Human Mutation|November 3, 2000
Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome populationM L Heritage, J C MacMillan, R P Colliton, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
The British Journal of Radiology|June 1, 1986
Technetium-99m Medronate uptake in subcutaneous soft-tissue nodules in a patient with renal failure and renal adenocarcinomaJ C MacMillan, S J Scott, M I McHugh, et al.
Journal of Telemedicine and Telecare|December 19, 2001
Telemedicine and clinical genetics: establishing a successful serviceM R Gattas, J C MacMillan, I Meinecke, et al.
Journal 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.
Annals of Surgical Oncology|October 13, 2001
Comparative expression of the mitotic regulators SAK and PLK in colorectal cancerJ C Macmillan, J W Hudson, S Bull, 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.
The Journal of Thoracic and Cardiovascular Surgery|February 1, 1978
Internal configuration of saphenous-coronary anastomoses as studied by the cast-injection techniqueJ N Young, J C MacMillan, I A May, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|September 30, 2005
A population genomics overview of the neuronal nitric oxide synthase (nNOS) gene and its relationship to migraine susceptibilityM P Johnson, R A Lea, N J Colson, 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.
Biochemical Society Transactions|November 1, 1995
Characterising the Huntington's disease gene productJ Wood, J C MacMillan, P Thomas, et al.
Human Mutation|November 3, 2000
Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome populationM L Heritage, J C MacMillan, R P Colliton, et al.
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