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Results: 4

Authors: Aartsma-Rus, Annemieke Janson, Anneke A.M. Kaman, Wendy E. Bremmer-Bout, Mattie Ommen, Gert-Jan B., Van den Dunnen, Johan T. Deutekom, Judith C.T., Van
Citation: Aartsma-rus, Annemieke et al., Antisense-Induced Multiexon Skipping for Duchenne Muscular Dystrophy Makes More Sense, American journal of human genetics , 74(1), 2004, pp. 83-92

Authors: White, Stefan Kalf, Margot Liu, Qiang Villerius, Michel Engelsma, Dieuwke Kriek, Marjolein Vollebregt, Ellen Bakker, Bert van Ommen, Gert-Jan B. Breuning, Martijn H. den Dunnen, Johan T.
Citation: White, Stefan et al., Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe Hybridization, American journal of human genetics , 71(2), 2002, pp. 365-374

Authors: Roelfsema, Jeroen H. White, Stefan J. Ariyürek, Yavuz Bartholdi, Deborah Niedrist, Dunja Papadia, Francesco Bacino, Carlos A. den Dunnen, Johan T. van Ommen, Gert-Jan B. Breuning, Martijn H. Hennekam, Raoul C: Peters, Dorien J.M.
Citation: H. Roelfsema, Jeroen et al., Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease, American journal of human genetics , 76(4), 2005, pp. 572-580

Authors: de Greef, Jessica C. Wang, Jun Balog, Judit den Dunnen, Johan T. van der Maarel, Silvère M.
Citation: C. De Greef, Jessica et al., Mutations in ZBTB24 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2, American journal of human genetics (Online) AJHG , 88(6), 2011, pp. 796-804
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