RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome von Blaydon, Diana C., Etheridge, Sarah L., Risk, Janet M., Hennies, Hans-Christian, Gay, Laura J., Carroll, Rebecca, Plagnol, Vincent, McRonald, Fiona E., Stevens, Howard P., Spurr, Nigel K., Bishop, D. Timothy, Ellis, Anthony, Jankowski, Janusz, Field, John K., Leigh, Irene M., South, Andrew P., Kelsell, David P.

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A null mutation in the Bacillus subtilis aconitase gene causes a block in Spo0A-phosphate-dependent gene expression von Craig, J E, Ford, M J, Blaydon, D C, Sonenshein, A L

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The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UK von Blaydon, DC, Mueller, RF, Hutchin, TP, Leroy, BP, Bhattacharya, SS, Bird, AC, Malcolm, S, Bitner-Glindzicz, M

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Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions von Pigors, M, Sarig, O, Heinz, L, Plagnol, V, Fischer, J, Mohamad, J, Malchin, N, Rajpopat, S, Kharfi, M, Lestringant, GG, Sprecher, E, Kelsell, DP, Blaydon, DC

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