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

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

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Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence von Tuckerman, E, Webb, T, Bundey, S E

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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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Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion von Renwick, J H, Bundey, S E, Ferguson-Smith, M A, Izatt, M M

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Population incidence and segregation ratios in the Martin-Bell syndrome von Webb, Tessa P., Bundey, Sarah E., Thake, Ann I., Todd, June, Opitz, John M., Reynolds, James F.

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Concordance in a sample of index cases and their monozygous twins and in the population of monozygous twin pairs von Chase, G A, Bundey, S E

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A clinical and molecular genetic study of dentatorubropallidolyusian 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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Clinical Genetics von Bundey, Sarah E

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The inheritance of otosclerosis von Morrison, A. W., Bundey, Sarah E.

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Single Amino Acid Mutation Contributes to Adaptive Beach Mouse Color Pattern von Hoekstra, Hopi E, Hirschmann, Rachel J, Bundey, Richard A, Insel, Paul A, Crossland, Janet P

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Integrated Quantum Mechanical and Machine Learning Methods Enable Scalable and General pKa Prediction for Pharmacokinetic Modeling von Walden, Daniel M., Bundey, Yogesh, Brunk, Nicholas E., Khotimchenko, Maksim, Hou, Hypatia, Chakravarty, Kaushik, Hixon, Mark S., Varshney, Jyotika

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12-Lipoxygenase in Opioid-Induced Delayed Cardioprotection: Gene Array, Mass Spectrometric, and Pharmacological Analyses von Patel, Hemal H, Fryer, Ryan M, Gross, Eric R, Bundey, Richard A, Hsu, Anna K, Isbell, Marilyn, Eusebi, Leonard O.V, Jensen, Roderick V, Gullans, Steven R, Insel, Paul A, Nithipatikom, Kasem, Gross, Garrett J

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Coordinate Down-regulation of Adenylyl Cyclase Isoforms and the Stimulatory G Protein (Gs) in Intestinal Epithelial Cell Differentiation von Choi, Lillian J., Jenikova, Gabriela, Hanson, Elaine, Spehlmann, Martina E., Boehling, Nicholas S., Kirstein, Shelli L., Bundey, Richard A., Smith, Jennifer R., Insel, Paul A., Eckmann, Lars

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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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A Novel Mechanism of Aberrant Pre-mRNA Splicing in Humans von Cogan, Joy D., Prince, Melissa A., Lekhakula, Somsong, Bundey, Sarah, Futrakul, Aree, McCarthy, Eleanor M. S., Phillips, John A.

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