DNA hypermethylation/boundary control loss identified in retinoblastomas associated with genetic and epigenetic inactivation of the RB1 gene promoter von Raizis, AM, Racher, HM, Foucal, A, Dimaras, H, Gallie, BL, George, PM

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Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells von REEVE, A. E, SIH, S. A, RAIZIS, A. M, FEINBERG, A. P

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Novel inactivating mutation of the calcium-sensing receptor in a young woman with mild hypercalcaemia von Kim, D. D. W., Que, L., Raizis, A. M., Florkowski, C. M.

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Effect of nonsense mutations on PTEN mRNA stability von RAIZIS, A. M, FERGUSON, M. M, GEORGE, P. M

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A Bisulfite Method of 5-Methylcytosine Mapping That Minimizes Template Degradation von Raizis, A.M., Schmitt, F., Jost, J.P.

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Structural analysis of the human insulin-like growth factor-II P3 promoter von RAIZIS, A. M, ECCLES, M. R, REEVE, A. E

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The characterization of ovine genes for atrial, brain, and C-type natriuretic peptides von Aitken, G.D, Raizis, A.M, Yandle, T.G, George, P.M, Espiner, E.A, Cameron, V.A

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Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndrome von Raizis, A M, Ferguson, M M, Robinson, B A, Atkinson, C H, George, P M

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A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13 von RAIZIS, A. M, BECROFT, D. M, SHAW, R. L, REEVE, A. E

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A Novel 5′ (40^41insA) Mutation in a Patient with Numerous Manifestations of Cowden Disease von Raizis, Anthony M., Ferguson, Martin M., Nicholls, David T., Goodisson, Derek W., George, Peter M.

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Effect of nonsense mutations on PTEN mRNA stability von Raizis, A M, Ferguson, M M, George, P M

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DNA hypermethylation/boundary control loss identified in retinoblastomas associated with genetic and epigenetic inactivation of the RB1 gene promoter von Raizis, AM, Racher, HM, Foucal, A, Dimaras, H, Gallie, BL, George, PM

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Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies von Rushlow, Diane E, BSc, Mol, Berber M, MSc, Kennett, Jennifer Y, MSc, Yee, Stephanie, MSc, Pajovic, Sanja, PhD, Thériault, Brigitte L, PhD, Prigoda-Lee, Nadia L, MSc, Spencer, Clarellen, BSc, Dimaras, Helen, PhD, Corson, Timothy W, PhD, Pang, Renée, MA, Massey, Christine, MSc, Godbout, Roseline, Prof, Jiang, Zhe, BSc, Zacksenhaus, Eldad, PhD, Paton, Katherine, MD, Moll, Annette C, MD, Houdayer, Claude, PhD, Raizis, Anthony, PhD, Halliday, William, MD, Lam, Wan L, Prof, Boutros, Paul C, PhD, Lohmann, Dietmar, Prof, Dorsman, Josephine C, PhD, Gallie, Brenda L, Prof

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Trilateral Retinoblastoma in a Patient With Peutz-Jeghers Syndrome von Raizis, Anthony M., Van Mater, David, Aaltonen, Lauri A., Lohmann, Dietmar, Cheale, Michelle S., Bickley, Vivienne M., George, Peter M., Zhou, Yaolin, Rosoff, Philip M.

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Spectrum of MECP2 mutations in New Zealand Rett syndrome patients von Raizis, Anthony M

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Trilateral Retinoblastoma in a Patient With Peutz– J eghers Syndrome von Raizis, Anthony M., Van Mater, David, Aaltonen, Lauri A., Lohmann, Dietmar, Cheale, Michelle S., Bickley, Vivienne M., George, Peter M., Zhou, Yaolin, Rosoff, Philip M.

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Role of genetic testing in retinoblastoma management at a tertiary referral centre von Pradhan, Monika A, Ng, Yvonne, Strickland, Adrienne, George, Peter M, Raizis, Anthony, Warrington, Jenny, Vincent, Andrea L

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To imeroloyio tou Ekmayiou: Hroniko mias apotihias / O anorthophrafos epiphrafopios von Raizis, M Byron

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The Complete Poems von Raizis, M. Byron, Vafopoulos, George, Nairn, Thom, Zervanou, Dionysia

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Poems von Raizis, M. Byron, Christianópoulos, Dínos, Kostís, Nicholas

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