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S Bundey

Showing results (81-90 of 99) with videos related to

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Journal of Medical Genetics|June 4, 1998
A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UKA C Hutchesson, S Bundey, M A Preece, et al.
Journal of Pediatric Ophthalmology and Strabismus|April 20, 2001
Rufous albinismJ S Mehta, P Good, D Maharaj, et al.
The British Journal of Ophthalmology|March 1, 1993
X linked exudative vitreoretinopathy: clinical features and genetic linkage analysisP Fullwood, J Jones, S Bundey, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Mitochondrial abnormalities in the DIDMOAD syndromeS Bundey, K Poulton, H Whitwell, et al.
Archives of Insect Biochemistry and Physiology|March 26, 2003
Eicosanoid involvement in the regulation of behavioral fever in the desert locust, Schistocerca gregariaS Bundey, S Raymond, P Dean, et al.
The New England Journal of Medicine|February 24, 1994
Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinismS T Lee, R D Nicholls, S Bundey, et al.
Journal of Medical Genetics|January 1, 1997
Fragile X syndrome is less common than previously estimatedJ E Morton, S Bundey, T P Webb, et al.
Eye (London, England)|January 1, 1996
ERG and EOG abnormalities in carriers of X-linked retinitis pigmentosaP Stavrou, P A Good, E J Broadhurst, et al.
The Quarterly Journal of Medicine|November 1, 1993
Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) geneM G Sweeney, S Bundey, M Brockington, et al.
Journal of Medical Genetics|January 1, 1988
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosomeK E Davies, T J Smith, S Bundey, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|June 4, 1998
A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UKA C Hutchesson, S Bundey, M A Preece, et al.
Journal of Pediatric Ophthalmology and Strabismus|April 20, 2001
Rufous albinismJ S Mehta, P Good, D Maharaj, et al.
The British Journal of Ophthalmology|March 1, 1993
X linked exudative vitreoretinopathy: clinical features and genetic linkage analysisP Fullwood, J Jones, S Bundey, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Mitochondrial abnormalities in the DIDMOAD syndromeS Bundey, K Poulton, H Whitwell, et al.
Archives of Insect Biochemistry and Physiology|March 26, 2003
Eicosanoid involvement in the regulation of behavioral fever in the desert locust, Schistocerca gregariaS Bundey, S Raymond, P Dean, et al.
The New England Journal of Medicine|February 24, 1994
Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinismS T Lee, R D Nicholls, S Bundey, et al.
Journal of Medical Genetics|January 1, 1997
Fragile X syndrome is less common than previously estimatedJ E Morton, S Bundey, T P Webb, et al.
Eye (London, England)|January 1, 1996
ERG and EOG abnormalities in carriers of X-linked retinitis pigmentosaP Stavrou, P A Good, E J Broadhurst, et al.
The Quarterly Journal of Medicine|November 1, 1993
Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) geneM G Sweeney, S Bundey, M Brockington, et al.
Journal of Medical Genetics|January 1, 1988
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosomeK E Davies, T J Smith, S Bundey, et al.
Pageof 10