Connexin 26 mutations in hereditary non-syndromic sensorineural deafness von Kelsell, D. P., Dunlop, J., Stevens, H. P., Lench, N. J., Liang, J. N., Parry, G., Mueller, R. F., Leigh, I. M.

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Analysis of the IBD5 locus and potential gene-gene interactions in Crohn’s disease von Negoro, K, McGovern, D P B, Kinouchi, Y, Takahashi, S, Lench, N J, Shimosegawa, T, Carey, A, Cardon, L R, Jewell, D P, van Heel, D A

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Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter von Jackson, Andrew P., McHale, Duncan P., Campbell, David A., Jafri, Hussain, Rashid, Yasmin, Mannan, Jovaria, Karbani, Gulshan, Corry, Peter, Levene, Malcolm I., Mueller, Robert F., Markham, Alexander F., Lench, Nicholas J., Woods, C. Geoffrey

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Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss von Scott, DA, Kraft, ML, Carmi, R, Ramesh, A, Elbedour, K, Yairi, Y, Srisailapathy, C. R. Srikumari, Rosengren, SS, Markham, AF, Mueller, RF, Lench, NJ, Van Camp, G, Smith, RJH, Sheffield, VC

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A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment von Hutchin, T P, Parker, M J, Young, I D, Davis, A C, Pulleyn, L J, Deeble, J, Lench, N J, Markham, A F, Mueller, R F

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A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34 von Moynihan, Leanne, Jackson, Andrew P., Roberts, Emma, Karbani, Gulshan, Lewis, Ian, Corry, Peter, Turner, Gwen, Mueller, Robert F., Lench, Nicholas J., Woods, C. Geoffrey

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Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF-κB transcription factors von van Heel, David A., Udalova, Irina A., De Silva, Arjuna P., McGovern, Dermot P., Kinouchi, Yoshitaka, Hull, Jeremy, Lench, Nicholas J., Cardon, Lon R., Carey, Alisoun H., Jewell, Derek P., Kwiatkowski, Dominic

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Characterisation of human patched germ line mutations in naevoid basal cell carcinoma syndrome von LENCH, N. J, TELFORD, E. A. R, HIGH, A. S, MARKHAM, A. F, WICKING, C, WAINWRIGHT, B. J

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Extent and Distribution of Linkage Disequilibrium in Three Genomic Regions von Abecasis, Gonçalo R., Noguchi, Emiko, Heinzmann, Andrea, Traherne, James A., Bhattacharyya, Sumit, Leaves, Nicholas I., Anderson, Gavin G., Zhang, Youming, Lench, Nicholas J., Carey, Alisoun, Cardon, Lon R., Moffatt, Miriam F., Cookson, William O.C.

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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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Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings von Mueller, R.F, Nehammer, A, Middleton, A, Houseman, M, Taylor, G.R, Bitner-Glindzciz, M, Van Camp, G, Parker, M, Young, I.D, Davis, A, Newton, V.E, Lench, N.J

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Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene von Denoyelle, Françoise, Weil, Dominique, Maw, Marion A., Wilcox, Stephen A., Lench, Nicholas J., Allen-Powell, Denise R., Osborn, Amelia H., Dahl, Hans-Henrik M., Middleton, Anna, Houseman, Mark J., Dodé, Catherine, Marlin, Sandrine, Boulila-ElGaïed, Amel, Grati, Mohammed, Ayadi, Hammadi, BenArab, Saïda, Bitoun, Pierre, Lina-Granade, Geneviève, Godet, Jacqueline, Mustapha, Mirna, Loiselet, Jacques, El-Zir, Élie, Aubois, Anne, Joannard, Alain, Levilliers, Jacqueline, Garabédian, Éréa-Noël, Mueller, Robert F., McKinlay Gardner, R. J., Petit, Christine

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A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2) von Lench, N J, Markham, A F, Mueller, R F, Kelsell, D P, Smith, R J, Willems, P J, Schatteman, I, Capon, H, Van De Heyning, P J, Van Camp, G

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A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22 von Campbell, D A, McHale, D P, Brown, K A, Moynihan, L M, Houseman, M, Karbani, G, Parry, G, Janjua, A H, Newton, V, al-Gazali, L, Markham, A F, Lench, N J, Mueller, R F

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The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants von van Heel, David A., Dechairo, Bryan M., Dawson, Gary, McGovern, Dermot P.B., Negoro, Kenichi, Carey, Alisoun H., Cardon, Lon R., Mackay, Ian, Jewell, Derek P., Lench, Nicholas J.

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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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Molecular analysis for genetic counselling in amelogenesis imperfecta von Aldred, MJ, Hall, RK, Kilpatrick, N, Bankier, A, Savarirayan, R, Lamandé, SR, Lench, NJ, Crawford, PJM

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A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands von ESTIVILL, X, FARRALL, M, WATSON, E. K, WILLIAMSON, R, WAINWRIGHT, B. J, SCAMBLER, P. J, BELL, G. M, HAWLEY, K. M. F, LENCH, N. J, BATES, G. P, KRUYER, H. C, FREDERICK, P. A, STANIER, P

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A gene for ataxic cerebral palsy maps to chromosome 9p12-q12 von McHale, D P, Jackson, A P, Campbell, Levene, M I, Corry, P, Woods, C G, Lench, N J, Mueller, R F, Markham, A F

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The human gene encoding FKBP-rapamycin associated protein (FRAP) maps to chromosomal band 1p36.2 von LENCH, N. J, MACADAM, R, MARKHAM, A. F

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