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G A Nicholson

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Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|December 8, 2015
Transanal rectal resection: an initial experience of 20 casesN C Buchs, G A Nicholson, T Yeung, et al.
Nature Genetics|November 1, 1993
De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)K Hayasaka, M Himoro, Y Sawaishi, et al.
Postgraduate Medical Journal|December 1, 1974
Gonococcaemia with arthritis, dermatitis and myocarditisH S Fraser, A L Liburd, J P Figueroa, et al.
Neurology|February 9, 2005
Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth lociA Kochanski, M Kennerson, M Kawulak, et al.
Neurogenetics|March 25, 2000
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA geneS M Forrest, M Knight, M B Delatycki, et al.
Annals of Neurology|October 1, 1977
Pedigree testing in Duchenne muscular dystrophyA D Roses, M J Roses, B S Metcalf, et al.
Journal of the Neurological Sciences|December 1, 1985
Variable distributions of serum creatine kinase reference values. Relationship to exercise activityG A Nicholson, J G McLeod, G Morgan, et al.
Nature Genetics|May 1, 1996
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3G A Nicholson, J L Dawkins, I P Blair, et al.
Lancet (London, England)|January 23, 1993
Explanation for exclusive maternal origin for congenital form of myotonic dystrophyJ C Mulley, A Staples, A Donnelly, et al.
Neurobiology of Disease|November 1, 1994
The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14qG Stevanin, P S Sousa, G Cancel, et al.
Pageof 12

Showing results (91-100 of 115) with videos related to

Sort By:
Pageof 12
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|December 8, 2015
Transanal rectal resection: an initial experience of 20 casesN C Buchs, G A Nicholson, T Yeung, et al.
Nature Genetics|November 1, 1993
De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)K Hayasaka, M Himoro, Y Sawaishi, et al.
Postgraduate Medical Journal|December 1, 1974
Gonococcaemia with arthritis, dermatitis and myocarditisH S Fraser, A L Liburd, J P Figueroa, et al.
Neurology|February 9, 2005
Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth lociA Kochanski, M Kennerson, M Kawulak, et al.
Neurogenetics|March 25, 2000
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA geneS M Forrest, M Knight, M B Delatycki, et al.
Annals of Neurology|October 1, 1977
Pedigree testing in Duchenne muscular dystrophyA D Roses, M J Roses, B S Metcalf, et al.
Journal of the Neurological Sciences|December 1, 1985
Variable distributions of serum creatine kinase reference values. Relationship to exercise activityG A Nicholson, J G McLeod, G Morgan, et al.
Nature Genetics|May 1, 1996
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3G A Nicholson, J L Dawkins, I P Blair, et al.
Lancet (London, England)|January 23, 1993
Explanation for exclusive maternal origin for congenital form of myotonic dystrophyJ C Mulley, A Staples, A Donnelly, et al.
Neurobiology of Disease|November 1, 1994
The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14qG Stevanin, P S Sousa, G Cancel, et al.
Pageof 12