A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN von Lehmann, K., Seemann, P., Silan, F., Goecke, T.O., Irgang, S., Kjaer, K.W., Kjaergaard, S., Mahoney, M.J., Morlot, S., Reissner, C., Kerr, B., Wilkie, A.O.M., Mundlos, S.

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Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism von Twigg, S.R.F., Ousager, L.B., Miller, K.A., Zhou, Y., Elalaoui, S.C., Sefiani, A., Bak, G.S, Hove, H., Hansen, L.K., Fagerberg, C.R., Tajir, M., Wilkie, A.O.M.

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Cellular evidence for selfish spermatogonial selection in aged human testes von Maher, G. J., Goriely, A., Wilkie, A. O. M.

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Genetic screening of 202 individuals with congenital limb malformations and requiring reconstructive surgery von Furniss, D, Kan, S-h, Taylor, I B, Johnson, D, Critchley, P S, Giele, H P, Wilkie, A O M

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Fgfr1 and Fgfr2 have distinct differentiation- and proliferation-related roles in the developing mouse skull vault von Iseki, S, Wilkie, A O, Morriss-Kay, G M

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Ethical review of research into rare genetic disorders von Parker, M, Ashcroft, R, Wilkie, A O M, Kent, A

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Fibroblast growth factor receptor 3 (FGFR3) mutation in a verrucous epidermal naevus associated with mild facial dysmorphism von Collin, B., Taylor, I.B., Wilkie, A.O.M., Moss, C.

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Craniosynostosis: Genes and Mechanisms von WILKIE, A. O. M

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Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1 von van den Elzen, M E P, Twigg, S R F, Goos, J A C, Hoogeboom, A J M, van den Ouweland, A M W, Wilkie, A O M, Mathijssen, I M J

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Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome von SLANEY, S. F, OLDRIDGE, M, HURST, J. A, MORRISS-KAY, G. M, HALL, C. M, POOLE, M. D, WILKIE, A. O. M

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A Review of the Molecular Genetics of the Human α-Globin Gene Cluster von Higgs, D.R., Vickers, M.A., Wilkie, A.O.M., Pretorius, I.M., Jarman, A.P., Weatherall, D.J.

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Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2 von Jeffery, Steve, Afzal, Ali R, Rajab, Anna, Fenske, Christiane D, Oldridge, Michael, Elanko, Navaratnam, Ternes-Pereira, Eliana, Tüysüz, Beyhan, Murday, Victoria A, Patton, Michael A, Wilkie, Andrew O.M

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Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification von Wilkie, Andrew O.M, Tang, Zequn, Elanko, Navaratnam, Walsh, Sinead, Twigg, Stephen R.F, Hurst, Jane A, Wall, Steven A, Chrzanowska, Krystyna H, Maxson, Robert E

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Cellular correlates of selfish spermatogonial selection von Maher, G. J., Rajpert‐De Meyts, E., Goriely, A., Wilkie, A. O. M.

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Apert Syndrome Mutations in Fibroblast Growth Factor Receptor 2 Exhibit increased Affinity for FGF Ligand von Anderson, Jane, Burns, Helen D., Enriquez-Harris, Pita, Wilkie, Andrew O. M., Heath, John K.

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Dominant mutations in ROR2 , encoding an orphan receptor tyrosine kinase, cause brachydactyly type B von Mansour, Sahar, Pollitt, Christine, Kimble, Robert B, Maringa, Monika, Oldridge, Michael, M Fortuna, Ana, Valenzuela, David M, DeChiara, Thomas M, Wilkie, Andrew O.M, Propping, Peter, Yancopoulos, George D

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The molecular basis of genetic dominance von Wilkie, A O

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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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Paternal Origin of FGFR2 Mutations in Sporadic Cases of Crouzon Syndrome and Pfeiffer Syndrome von Glaser, Rivka L., Jiang, Wen, Boyadjiev, Simeon A., Tran, Alissa K., Zachary, Andrea A., Van Maldergem, Lionel, Johnson, David, Walsh, Sinead, Oldridge, Michael, Wall, Steven A., Wilkie, Andrew O.M., Jabs, Ethylin Wang

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The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation von Flint, Jonathan, Wilkie, Andrew O.M, Buckle, Veronica J, Winter, Robin M, Holland, Anthony J, McDermid, Heather E

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