Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome von Reardon, William, Winter, Robin M, Rutland, Paul, Pulleyn, Louise J, Jones, Barry M, Malcolm, Sue

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A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome von Muenke, Maximilian, Schell, Ute, Hehr, Andreas, Robin, Nathaniel H, Losken, H. Wolfgang, Schinzel, Albert, Pulleyn, Louise J, Rutland, Paul, Reardon, William, Malcolm, Sue, Winter, Robin M

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Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes von Rutland, Paul, Pulleyn, Louise J, Reardon, William, Baraitser, Michael, Hayward, Richard, Jones, Barry, Malcolm, Sue, Winter, Robin M, Oldridge, Michael, Slaney, Sarah F, Poole, Michael D, Wilkie, Andrew O.M

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TGFβ1 allele association with asthma severity von PULLEYN, Louise J, NEWTON, Robert, ADCOCK, Ian M, BARNES, Peter J

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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome von Wilkie, Andrew O.M, Slaney, Sarah F, Oldridge, Michael, Poole, Michael D, Ashworth, Geraldine J, Hockley, Anthony D, Hayward, Richard D, David, David J, Pulleyn, Louise J, Rutland, Paul, Malcolm, Susan, Winter, Robin M, Reardon, William

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Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis von Reardon, W, Wilkes, D, Rutland, P, Pulleyn, L J, Malcolm, S, Dean, J C, Evans, R D, Jones, B M, Hayward, R, Hall, C M, Nevin, N C, Baraister, M, Winter, R M

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Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus von Pulleyn, L J, Reardon, W, Wilkes, D, Rutland, P, Jones, B M, Hayward, R, Hall, C M, Brueton, L, Chun, N, Lammer, E, Malcolm, S, Winter, R M

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A novel mutation in the mitochondrial tRNASer(UCN) gene in a family with non-syndromic sensorineural hearing impairment von Hutchin, Tim P, Parker, Mick J, Young, Ian D, Davis, Adrian C, Pulleyn, Louise J, Deeble, Jayne, Lench, Nicholas J, Markham, Alex F, Mueller, Robert F

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A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome von Muenke, Maximilian, Schell, Ute, Hehr, Andreas, Robin, Nathaniel H, Losken, H Wolfgang, Schinzel, Albert, Pulleyn, Louise J, Rutland, Paul, Reardon, William, Malcolm, Sue, Winter, Robin M

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Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma von Cookson, William O C M, Zhang, Youming, Leaves, Nicholas I, Anderson, Gavin G, Ponting, Chris P, Broxholme, John, Holt, Richard, Edser, Pauline, Bhattacharyya, Sumit, Dunham, Andy, Adcock, Ian M, Pulleyn, Louise, Barnes, Peter J, Harper, John I, Abecasis, Gonçalo, Cardon, Lon, White, Melanie, Burton, John, Matthews, Lucy, Mott, Richard, Ross, Mark, Cox, Roger, Moffatt, Miriam F

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