Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2 von Hever, AM, Williamson, KA, Van Heyningen, V

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Pax6 Controls Progenitor Cell Identity and Neuronal Fate in Response to Graded Shh Signaling von Ericson, J, Rashbass, P, Schedl, A, Brenner-Morton, S, Kawakami, A, van Heyningen, V, Jessell, T.M, Briscoe, J

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FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic Abnormality von Fantes, J.A., Boland, E., Ramsay, J., Donnai, D., Splitt, M., Goodship, J.A., Stewart, H., Whiteford, M., Gautier, P., Harewood, L., Holloway, S., Sharkey, F., Maher, E., van Heyningen, V., Clayton-Smith, J., Fitzpatrick, D.R., Black, G.C.M.

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PAX6 in sensory development von van Heyningen, Veronica, Williamson, Kathleen A.

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Role of Pax6 in development of the cerebellar system von Engelkamp, D, Rashbass, P, Seawright, A, van Heyningen, V

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Mechanisms of non-Mendelian inheritance in genetic disease von van Heyningen, Veronica, Yeyati, Patricia L.

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National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology von Morrison, D, FitzPatrick, D, Hanson, I, Williamson, K, van Heyningen, V, Fleck, B, Jones, I, Chalmers, J, Campbell, H

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Zinc Finger Point Mutations Within the WT1 Gene in Wilms Tumor Patients von Little, M. H., Prosser, J., Condie, A., Smith, P. J., Van Heyningen, V., Nastie, N. D.

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Wilms' tumour: reconciling genetics and biology von Van Heyningen, Veronica, Hastie, Nicholas D

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Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization von FANTES, J. A, BICKMORE, W. A, FLETCHER, J. M, BALLESTA, F, HANSON, M, VAN HEYNINGEN, V

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Phenotypic Variability and Asymmetry of Rieger Syndrome Associated with PITX2 Mutations von Perveen, Rahat, Lloyd, I. Christopher, Clayton-Smith, Jill, Churchill, Amanda, van Heyningen, Veronica, Hanson, Isabel, Taylor, David, McKeown, Carole, Super, Maurice, Kerr, Bronwyn, Winter, Robin, Black, Graeme C. M

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Hemolytic uremic syndrome associated with Denys-Drash syndrome von SHERBOTIE, J. R, VAN HEYNINGEN, V, AXTON, R, WILLIAMSON, K, FINN, L. S, KAPLAN, B. S

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Cognitive functioning in humans with mutations of the PAX6 gene von THOMPSON, P. J, MITCHELL, T. N, FREE, S. L, WILLIAMSON, K. A, HANSON, I. M, VAN HEYNINGEN, V, MOORE, A. T, SISODIYA, S. M

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In utero nephropathy, Denys-Drash syndrome and Potter phenotype von MAALOUF, E. F, FERGUSON, J, VAN HEYNINGEN, V, MODI, N

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PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation von Malandrini, A, Mari, F, Palmeri, S, Gambelli, S, Berti, G, Bruttini, M, Bardelli, AM, Williamson, K, Van Heyningen, V, Renieri, A

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Role for the Wilms Tumor Gene in Genital Development? von Van Heyningen, V., Bickmore, W. A., Seawright, A., Fletcher, J. M., Maule, J., Fekete, G., Gessler, M., Bruns, G. A. P., Huerre-Jeanpierre, C., Junien, C., Williams, B. R. G., Hastie, N. D.

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Modulation of DNA Binding Specificity by Alternative Splicing of the Wilms Tumor wt1 Gene Transcript von Bickmore, W. A., Oghene, K., Little, M. H., Seawright, A., van Heyningen, V., Hastie, N. D.

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Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma von JAMIESON, Robyn V, PERVEEN, Rahat, BLACK, Graeme C. M, KERR, Bronwyn, CARETTE, Martin, YARDLEY, Jill, HEON, Elise, WIRTH, M. Gabriela, VAN HEYNINGEN, Veronica, DONNAI, Di, MUNIER, Francis

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Pax6 is required to regulate the cell cycle and the rate of progression from symmetrical to asymmetrical division in mammalian cortical progenitors von Estivill-Torrus, Guillermo, Pearson, Helen, van Heyningen, Veronica, Price, David J, Rashbass, Penny

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PAX6 mutations reviewed von Prosser, Jane, van Heyningen, Veronica

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