Showing 1 - 20 results of 27 for search 'van Ommen, T', query time: 0.04s
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Identity, (Dis)Ability and Belonging: Liturgy and Worship through the Lens of Autism by Armand Léon van Ommen
Published 2024-12-01
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Ідентичність, (не)спроможність та приналежність: літургія та поклоніння крізь призму аутизму by Armand Léon van Ommen
Published 2024-12-01
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Enhanced exon-skipping induced by U7 snRNA carrying a splicing silencer sequence: Promising tool for DMD therapy. by Goyenvalle, A, Babbs, A, van Ommen, G, Garcia, L, Davies, K
Published 2009Journal article -
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The Pathogenesis and Therapy of Muscular Dystrophies by Guiraud, S, Aartsma-Rus, A, Vieira, N, Davies, K, van Ommen, G, Kunkel, L
Published 2015Journal article -
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Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21. by Ho, M, Monaco, A, Blonden, L, van Ommen, G, Affara, N, Ferguson-Smith, M, Lehrach, H
Published 1992Journal article -
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A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene. by Burmeister, M, Monaco, A, Gillard, E, van Ommen, G, Affara, N, Ferguson-Smith, M, Kunkel, L, Lehrach, H
Published 1988Journal article -
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Hospital-associated venous thromboembolism in pediatrics: a systematic review and meta-analysis of risk factors and risk-assessment models by Arash Mahajerin, Brian R. Branchford, Ernest K. Amankwah, Leslie Raffini, Elizabeth Chalmers, C. Heleen van Ommen, Neil A. Goldenberg
Published 2015-08-01
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A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome. by van Ommen, G, Verkerk, J, Hofker, M, Monaco, A, Kunkel, L, Ray, P, Worton, R, Wieringa, B, Bakker, E, Pearson, P
Published 1986Journal article -
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Generation and characterization of transgenic mice with the full-length human DMD gene. by 't Hoen, P, de Meijer, E, Boer, J, Vossen, R, Turk, R, Maatman, R, Davies, K, van Ommen, G, van Deutekom, J, den Dunnen, J
Published 2008Journal article -
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Exploring transmission dynamics of the Sarcoptes scabiei mite in humans by combining molecular typing and epidemiological variables, the Netherlands 2016–2023 by Martijn Vink, Hester Coppoolse, Anneke Bergmans, Meike Wennekes, Suzan Pas, Jane Pattipeilohy-van Ommen, Marieta Braks, Sylvia Bruisten, Annemie Galimont-Collen, Bas Wintermans, Ewout Fanoy
Published 2024-10-01
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Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardation. by van der Maarel, S, Scholten, I, Maat-Kievit, J, Huber, I, de Kok, Y, de Wijs, I, van de Pol, T, van Bokhoven, H, den Dunnen, J, van Ommen, G
Published 1995Journal article -
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Association of mild kidney dysfunction with diastolic dysfunction and heart failure with preserved ejection fraction by Robin W. M. Vernooij, Anne‐Mar L. N. vanOmmen, Gideon B. Valstar, Maarten Jan Cramer, Arco J. Teske, Roxana Menken, Leo Hofstra, Frans H. Rutten, Michiel L. Bots, Hester M. denRuijter, Marianne C. Verhaar
Published 2024-02-01
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An Immune Response Network Associated with Blood Lipid Levels by Inouye, Michael, Silander, Kaisa, Hamalainen, Eija, Salomaa, Veikko, Harald, Kennet, Jousilahti, Pekka, Männistö, Satu, Eriksson, Johan G., Saarela, Janna, Ripatti, Samuli, Perola, Markus, van Ommen, Gert-Jan B., Taskinen, Marja-Riitta, Palotie, Aarno, Dermitzakis, Emmanouil T., Peltonen, Leena
Published 2011
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