Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome von Barrett, T.G, Bundey, S.E, Macleod, A.F

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Wolfram (DIDMOAD) syndrome von Barrett, T G, Bundey, S E

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Few psychological consequences of presymptomatic testing for Huntington disease von Bundey, Sarah

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Eicosanoid involvement in the regulation of behavioral fever in the desert locust, Schistocerca gregaria von Bundey, S., Raymond, S., Dean, P., Roberts, S.K., Dillon, R.J., Charnley, A.K.

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A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy von Chen, Z-Y, Battinelli, E.M, Fielder, A, Bundey, S, Sims, K, Breakefield, X.O, Craig, I.W

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Clinical and Genetic Features of Ataxia-telangiectasia von Bundey, S.

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Usher syndrome in the city of Birmingham—prevalence and clinical classification von Hope, C I, Bundey, S, Proops, D, Fielder, A R

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A Mutation (2314delG) in the Usher Syndrome Type IIA Gene: High Prevalence and Phenotypic Variation von Liu, Xue-Zhong, Hope, Carolyn, Liang, Chuan Yu, Zou, Jiu Mu, Xu, Li Rong, Cole, T., Mueller, Robert F., Bundey, Sarah, Nance, Walter, Steel, Karen P., Brown, Steve D.M.

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A Five-Year Prospective Study of the Health of Children in Different Ethnic Groups, with Particular Reference to the Effect of Inbreeding von Bundey, Sarah, Alam, Hasina

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Optic atrophy in Wolfram (DIDMOAD) syndrome von Barrett, Timothy G, Bundey, Sarah E, Fielder, Alistair R, Good, Peter A

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Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity von COLLIER, D. A, BARRETT, T. G, CURTIS, D, MACLEOD, A, ARRANZ, M. J, MAASSEN, J. A, BUNDEY, S

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A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK von Hutchesson, A C, Bundey, S, Preece, M A, Hall, S K, Green, A

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Fragile X syndrome is less common than previously estimated von Morton, J E, Bundey, S, Webb, T P, MacDonald, F, Rindl, P M, Bullock, S

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A Syndrome of Severe Mental Retardation, Spasticity, and Tapetoretinal Degeneration Linked to Chromosome 15q24 von Mitchell, S.J., McHale, D.P., Campbell, D.A., Lench, N.J., Mueller, R.F., Bundey, S.E., Markham, A.F.

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Autozygosity Mapping, to Chromosome 11q25, of a Rare Autosomal Recessive Syndrome Causing Histiocytosis, Joint Contractures, and Sensorineural Deafness von Moynihan, Leanne M., Bundey, Sarah E., Heath, David, Jones, E. Lynn, McHale, Duncan P., Mueller, Robert F., Markham, Alexander F., Lench, Nicholas J.

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A Gene for Autosomal Recessive Symmetrical Spastic Cerebral Palsy Maps to Chromosome 2q24-25 von McHale, D.P., Mitchell, S., Bundey, S., Moynihan, L., Campbell, D.A., Woods, C.G., Lench, N.J., Mueller, R.F., Markham, A.F.

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Clinical and genetic features of ataxia-telangiectasia von Bundey, S.

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A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four european families von Warner, T. T., Williams, L. D., Walker, R. W. H., Flinter, F., Robb, S. A., Bundey, S. E., Honavar, M., Harding, A. E.

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Unusual features in the inheritance of ataxia telangiectasia von WOODS, C. G, BUNDEY, S. E, TAYLOR, A. M. R

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Prevalence and type of cerebral palsy von Bundey, S

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