Yield of Molecular and Clinical Testing for Arrhythmia Syndromes: Report of 15 Years’ Experience by Hofman, Nynke, Tan, Hanno L., Alders, Mariëlle, Kolder, Iris, de Haij, Simone, Mannens, Marcel M.A.M., Lombardi, Maria Paola, dit Deprez, Ronald H. Lekanne, van Langen, Irene, Wilde, Arthur A.M.

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ABCB4 deficiency: A family saga of early onset cholelithiasis, sclerosing cholangitis and cirrhosis and a novel mutation in the ABCB4 gene by Denk, Gerald U., Bikker, Hennie, Lekanne dit Deprez, Ronald H., Terpstra, Valeska, Van Der Loos, Chris, Beuers, Ulrich, Rust, Christian, Pusl, Thomas

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Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications by van Rijsingen, Ingrid A.W, Bakker, Annemieke, Azim, Donija, Hermans-van Ast, Johanna F, van der Kooi, Anneke J, van Tintelen, J. Peter, van den Berg, Maarten P, Christiaans, Imke, Lekanne dit Deprez, Ronald H, Wilde, Arthur A.M, Zwinderman, Aeilko H, Meijers, Joost C.M, Grootemaat, Anita E, Nieuwland, Rienk, Pinto, Yigal M, Pinto-Sietsma, Sara-Joan

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Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogeni... by van der Zwaag, Paul A., van Rijsingen, Ingrid A.W., Asimaki, Angeliki, Jongbloed, Jan D.H., van Veldhuisen, Dirk J., Wiesfeld, Ans C.P., Cox, Moniek G.P.J., van Lochem, Laura T., de Boer, Rudolf A., Hofstra, Robert M.W., Christiaans, Imke, van Spaendonck-Zwarts, Karin Y., Lekanne dit Deprez, Ronald H., Judge, Daniel P., Calkins, Hugh, Suurmeijer, Albert J.H., Hauer, Richard N.W., Saffitz, Jeffrey E., Wilde, Arthur A.M., van den Berg, Maarten P., van Tintelen, J. Peter

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A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q by van de Meerakker, Judith B A, van Engelen, Klaartje, Mathijssen, Inge B, Lekanne dit Deprez, Ronald H, Lam, Jan, Wilde, Arthur A M, Baars, Marieke J H, Mannens, Marcel M A M, Mulder, Barbara J M, Moorman, Antoon F M, Postma, Alex V

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NF2 status of meningiomas is associated with tumour localization and histology by Kros, Johan, de Greve, Kitty, van Tilborg, Angela, Hop, Wim, Pieterman, Herman, Avezaat, Cees, Lekanne dit Deprez, Ronald, Zwarthoff, Ellen

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Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects by Vrijenhoek, Terry, Kraaijeveld, Ken, Elferink, Martin, de Ligt, Joep, Kranendonk, Elcke, Santen, Gijs, Nijman, Isaac J, Butler, Derek, Claes, Godelieve, Costessi, Adalberto, Dorlijn, Wim, van Eyndhoven, Winfried, Halley, Dicky J J, van den Hout, Mirjam C G N, van Hove, Steven, Johansson, Lennart F, Jongbloed, Jan D H, Kamps, Rick, Kockx, Christel E M, de Koning, Bart, Kriek, Marjolein, Lekanne Dit Deprez, Ronald, Lunstroo, Hans, Mannens, Marcel, Mook, Olaf R, Nelen, Marcel, Ploem, Corrette, Rijnen, Marco, Saris, Jasper J, Sinke, Richard, Sistermans, Erik, van Slegtenhorst, Marjon, Sleutels, Frank, van der Stoep, Nienke, van Tienhoven, Marianne, Vermaat, Martijn, Vogel, Maartje, Waisfisz, Quinten, Marjan Weiss, Janneke, van den Wijngaard, Arthur, van Workum, Wilbert, Ijntema, Helger, van der Zwaag, Bert, van IJcken, Wilfred F J, den Dunnen, Johan, Veltman, Joris A, Hennekam, Raoul, Cuppen, Edwin

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Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects by Vrijenhoek, Terry, Kraaijeveld, Ken, Elferink, Martin, de Ligt, Joep, Kranendonk, Elcke, Santen, Gijs, Nijman, Isaac J, Butler, Derek, Claes, Godelieve, Costessi, Adalberto, Dorlijn, Wim, van Eyndhoven, Winfried, Halley, Dicky J J, van den Hout, Mirjam C G N, van Hove, Steven, Johansson, Lennart F, Jongbloed, Jan D H, Kamps, Rick, Kockx, Christel E M, de Koning, Bart, Kriek, Marjolein, Deprez, Ronald Lekanne Dit, Lunstroo, Hans, Mannens, Marcel, Mook, Olaf R, Nelen, Marcel, Ploem, Corrette, Rijnen, Marco, Saris, Jasper J, Sinke, Richard, Sistermans, Erik, van Slegtenhorst, Marjon, Sleutels, Frank, van der Stoep, Nienke, van Tienhoven, Marianne, Vermaat, Martijn, Vogel, Maartje, Waisfisz, Quinten, Weiss, Janneke Marjan, van den Wijngaard, Arthur, van Workum, Wilbert, Ijntema, Helger, van der Zwaag, Bert, van IJcken, Wilfred F J, den Dunnen, Johan T, Veltman, Joris A, Hennekam, Raoul, Cuppen, Edwin

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Abstract 18381: Ten Years Genetic Screening in a Large Cohort of Patients with Dilated Cardiomyopathy by van Tintelen, Peter, Spaendonck-Zwarts, Karin Y, van Rijsingen, Ingrid A, Jongbloed, Jan D, Lekanne Dit Deprez, Ronald H, Post, Jan G, van Mil, Anneke, Christiaans, Imke, Wilde, Arthur A, van den Berg, Maarten P, Pinto, Yigal M

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Consensus recommendation on Fabry disease diagnosis in adult patients with left ventricular hypertrophy by Smid, Bouwien, van der Tol, Linda, Cecchi, Franco, Elliott, Perry, Hughes, Derralynn, Linthorst, Gabor, Timmermans, Janneke, Weidemann, Frank, West, Michael, Biegstraaten, Marieke, Deprez, Ronald Lekanne Dit, Florquin, Sandrine, Postema, Pieter, van der Wal, Allard, den Bergh Weerman, Marius van, Hollak, Carla

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Erratum: Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects by Vrijenhoek, Terry, Kraaijeveld, Ken, Elferink, Martin, de Ligt, Joep, Kranendonk, Elcke, Santen, Gijs, Nijman, Isaac J, Butler, Derek, Claes, Godelieve, Costessi, Adalberto, Dorlijn, Wim, van Eyndhoven, Winfried, Halley, Dicky JJ, van den Hout, Mirjam CGN, van Hove, Steven, Johansson, Lennart F, Jongbloed, Jan DH, Kamps, Rick, Kockx, Christel EM, de Koning, Bart, Kriek, Marjolein, Deprez, Ronald Lekanne dit, Lunstroo, Hans, Mannens, Marcel, Mook, Olaf R, Nelen, Marcel, Ploem, Corrette, Rijnen, Marco, Saris, Jasper J, Sinke, Richard, Sistermans, Erik, van Slegtenhorst, Marjon, Sleutels, Frank, van der Stoep, Nienke, van Tienhoven, Marianne, Vermaat, Martijn, Vogel, Maartje, Waisfisz, Quinten, Weiss, Janneke Marjan, van den Wijngaard, Arthur, van Workum, Wilbert, Ijntema, Helger, van der Zwaag, Bert, van IJcken, Wilfred FJ, den Dunnen, Johan T, Veltman, Joris A, Hennekam, Raoul, Cuppen, Edwin

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Abstract 2722: Large Scale Mutation Discovery Screen Identifies Functionally Variant UGDH Alleles in Patients with Atrioventricular Valve Defects by Bakkers, Jeroen, Chocron, Sonja, Gouriev, Victor, Smith, Kelly, Deprez, Ronald Lekanne dit, Joziasse, Irene C, Doevendans, Pieter A, Mulder, Barbara J, Simpson, Melanie, Barycki, Joseph, Cuppen, Edwin

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CDNA arrays: the ups and downs by Remme, C A, Lombardi, M P, van den Hoff, M J, Lekanne dit Deprez, R H

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