Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling von Turk, R, Sterrenburg, E, de Meijer, E J, van Ommen, G-J B, den Dunnen, J T, 't Hoen, P A C

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The Human Genome Project and the future of diagnostics, treatment and prevention von Ommen, G.‐J. B.

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Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency von Kiezun, Adam, Pulit, Sara L, Francioli, Laurent C, van Dijk, Freerk, Swertz, Morris, Boomsma, Dorret I, van Duijn, Cornelia M, Slagboom, P Eline, van Ommen, G J B, Wijmenga, Cisca, de Bakker, Paul I W, Sunyaev, Shamil R

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The Human Genome Project and the Role of Genetics in Health Care von VAN OMMEN, G.-J. B

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Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter von WIJMENGA, C, SANDKUIJL, L. A, FRANTS, R. R, MOERER, P, VAN DER BOORN, N, BODRUG, S. E, RAY, P. N, BROUWER, O. F, MURRAY, J. C, VAN OMMEN, G. J. B, PADBERG, G. W

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Deletion of the Caenorhabditis elegans homologues of the CLN3 gene, involved in human juvenile neuronal ceroid lipofuscinosis, causes a mild progeric phenotype von Voer, G., Bent, P., Rodrigues, A. J. G., Ommen, G.‐J. B., Peters, D. J. M., Taschner, P. E. M.

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Human genetics in health care von van Ommen, G J

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Limb-girdle muscular dystrophy in the Netherlands : Gene defect identified in half the families von VAN DER KOOI, A. J, FRANKHUIZEN, W. S, BAKKER, E, GINJAAR, H. B, BARTH, P. G, HOWELER, C. J, PADBERG, G. W, SPAANS, F, WINTZEN, A. R, WOKKE, J. H. J, VAN OMMEN, G.-J. B, DE VISSER, M

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Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells von Aartsma-Rus, A, Kaman, W E, Bremmer-Bout, M, Janson, A A M, den Dunnen, J T, van Ommen, G-J B, van Deutekom, J C T

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Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD) von Nadarajah, V.D, van Putten, M, Chaouch, A, Garrood, P, Straub, V, Lochmüller, H, Ginjaar, H.B, Aartsma-Rus, A.M, van Ommen, G.J.B, den Dunnen, J.T, t Hoen, P.A.C

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Fluorescent labelling of cRNA for microarray applications von ’t Hoen, Peter A. C., de Kort, Floor, van Ommen, G. J. B., den Dunnen, Johan T.

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Two-colour immunocytochemical staining of gamma (γ) and epsilon (ϵ) type haemoglobin in fetal red cells von Mesker, Wilma E., Ouwerkerk-V Velzen, Maria C. M., Oosterwijk, Jan C., Bernini, Luigi F., Golbus, Mitchell S., Kanhai, Humphrey H. H., Van Ommen, Gert Jan B., Tanke, Hans J.

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Genome Research: HUGO and Future Healthcare von van Ommen, Gert-Jan B

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WHSC1, a 90 kb SET Domain-Containing Gene, Expressed in Early Development and Homologous to a Drosophila Dysmorphy Gene Maps in the Wolf-Hirschhorn Syndrome Critical Region and is... von Stec, Ingrid, Wright, Tracy J., van Ommen, Gert-Jan B., de Boer, Piet A. J., van Haeringen, Arie, Moorman, Antoon F. M., Altherr, Michael R., den Dunnen, Johan T.

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Interruption of Perfect CAG Repeats by CAA Triplets Improves the Stability of Glutamine-Encoding Repeat Sequences von Dorsman, J.C, Bremmer-Bout, M, Pepers, B, Ommen, G.-J.B. van, Dunnen, J.T. Den

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Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMD von Roest, P A, Bout, M, van der Tuijn, A C, Ginjaar, I B, Bakker, E, Hogervorst, F B, van Ommen, G J, den Dunnen, J T

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Therapeutic Modulation of DMD Splicing by Blocking Exonic Splicing Enhancer Sites with Antisense Oligonucleotides von AARTSMA-RUS, A., JANSON, A.A.M., HEEMSKERK, J.A., DE WINTER, C.L., VAN OMMEN, G.-J.B., VAN DEUTEKOM, J.C.T.

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Screening for BRCA2 mutations in 81 Dutch breast–ovarian cancer families von Peelen, T, Vliet, M van, Bosch, A, Bignell, G, Vasen, H F A, Klijn, J G M, Meijers-Heijboer, H, Stratton, M, van Ommen, G-J B, Cornelisse, C J, Devilee, P

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Relative power and sample size analysis on gene expression profiling data von Iterson, M. van, Hoen, P.A.C. 't, Pedotti, P, Hooiveld, G.J.E.J, Dunnen, J.T. den, Ommen, G.J.B. van, Boer, J.M, Menezes, R.X

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Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16) von GILES, R. H, DAUWERSE, J. G, VAN OMMEN, G.-J. B, HAGEMEIJER, A, VAN DER REIJDEN, B. A, BREUNING, M. H, HIGGINS, C, PETRIJ, F, WESSELS, J. W, BEVERSTOCK, G. C, DÖHNER, H, JOTTERAND-BELLOMO, M, FALKENBURG, J. H. F, SLATER, R. M

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