Neural Basis of an Inherited Speech and Language Disorder von Vargha-Khadem, F., Watkins, K. E., Price, C. J., Ashburner, J., Alcock, K. J., Connelly, A., Frackowiak, R. S. J., Friston, K. J., Pembrey, M. E., Mishkin, M., Gadian, D. G., Passingham, R. E.

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Localisation of a gene implicated in a severe speech and language disorder von Fisher, Simon E, Vargha-Khadem, Faraneh, Monaco, Anthony P, Pembrey, Marcus E, Watkins, Kate E

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Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation von Knight, S.J.L., Flannery, A.V., Hirst, M.C., Campbell, L., Christodoulou, Z., Phelps, S.R., Pointon, J., Middleton-Price, H.R., Barnicoat, A., Pembrey, M.E., Holland, J., Oostra, B.A., Bobrow, M., Davies, K.E.

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Radiological malformations of the ear in pendred syndrome von Phelps, P.D., Coffey, R.A., Trembath, R.C., Luxon, L.M., Grossman, A.B., Britton, K.E., Kendall-Taylor, P., Graham, J.M., Cadge, B.C., Stephens, S.G.D., Pembrey, M.E., Reardon, W.

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Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA von Reardon, W., Pembrey, M.E., Trembath, R.C., Ross, R.J.M., Sweeney, M.G., Harding, A.E., Luxon, L.M.

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A clinical and genetic study of campomelic dysplasia von Mansour, S, Hall, C M, Pembrey, M E, Young, I D

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Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4 von Yvette J. M. de Kok, van der Maarel, Silvère M., Bitner-Glindzicz, Maria, Huber, Irene, Monaco, Anthony P., Malcolm, Susan, Pembrey, Marcus E., Ropers, Hans-Hilger, Frans P. M. Cremers

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Uniparental paternal disomy in Angelman's syndrome von Malcolm, S., Clayton-Smith, J., Nichols, M., Pembrey, M.E., Armour, J.A.L., Jeffreys, A.J., Robb, S., Webb, T.

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Angelman syndrome von Clayton-Smith, J, Pembrey, M E

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Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen von TYSON, Jessica, TRANEBJAERG, Lisbeth, PEMBREY, Marcus E, MALCOLM, Sue, BITNER-GLINDZICZ, Maria, MCENTAGART, Meriel, LARSEN, Lars A, CHRISTIANSEN, Michael, WHITEFORD, Margo L, BATHEN, Jørn, ASLAKSEN, Bjørn, SØRLAND, Svein Jan, LUND, Ole

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An assessment of screening strategies for fragile X syndrome in the UK von Pembrey, M E, Barnicoat, A J, Carmichael, B, Bobrow, M, Turner, G

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Association of the INS VNTR with size at birth von Dunger, David B, Ong, Ken K.L, Huxtable, Stewart J, Sherriff, Andrea, Woods, Kathryn A, Ahmed, Marion L, Golding, Jean, Pembrey, Marcus E, Ring, Sue, Bennett, Simon T, Todd, John A

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In the light of preimplantation genetic diagnosis: some ethical issues in medical genetics revisited von Pembrey, M E

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Molecular mechanisms in Angelman syndrome: a survey of 93 patients von Chan, C T, Clayton-Smith, J, Cheng, X J, Buxton, J, Webb, T, Pembrey, M E, Malcolm, S

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Mapping of DFN2 to Xq22 von TYSON, J, BELLMAN, S, NEWTON, V, SIMPSON, P, MALCOLM, S, PEMBREY, M. E, BITNER-GLINDZICZ, M

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Sex-specific, male-line transgenerational responses in humans von Pembrey, Marcus E, Bygren, Lars Olov, Kaati, Gunnar, Edvinsson, Sören, Northstone, Kate, Sjöström, Michael, Golding, Jean

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Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage von Gausden, E, Coyle, B, Armour, J A, Coffey, R, Grossman, A, Fraser, G R, Winter, R M, Pembrey, M E, Kendall-Taylor, P, Stephens, D, Luxon, L M, Phelps, P D, Reardon, W, Trembath, R

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Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome von Clayton-Smith, J, Webb, T, Cheng, X J, Pembrey, M E, Malcolm, S

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Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families von Gilbert, H L, Buxton, J L, Chan, C T, McKay, T, Cottrell, S, Ramsden, S, Winter, R M, Pembrey, M E, Malcolm, S

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A multipedigree linkage study of X-linked deafness: Linkage to Xq13-q21 and evidence for genetic heterogeneity von Reardon, W., Middleton-Price, H.R., Sandkuijl, L., Phelps, P., Bellman, S., Luxon, L., Pembrey, M.E., Malcolm, S.

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