A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation von Postma, Alex V, van de Meerakker, Judith B.A, Mathijssen, Inge B, Barnett, Phil, Christoffels, Vincent M, Ilgun, Aho, Lam, Jan, Wilde, Arthur A.M, Deprez, Ronald H. Lekanne, Moorman, Antoon F.M

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Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics von Mook, Olaf R F, Haagmans, Martin A, Soucy, Jean-François, van de Meerakker, Judith B A, Baas, Frank, Jakobs, Marja E, Hofman, Nynke, Christiaans, Imke, Lekanne Deprez, Ronald H, Mannens, Marcel M A M

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A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q von 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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A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding von van de Meerakker, Judith B.A., Christiaans, Imke, Barnett, Phil, Lekanne Deprez, Ronald H., Ilgun, Aho, Mook, Olaf R.F., Mannens, Marcel M.A.M., Lam, Jan, Wilde, Arthur A.M., Moorman, Antoon F.M., Postma, Alex V.

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Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly von Postma, Alex V, van Engelen, Klaartje, van de Meerakker, Judith, Rahman, Thahira, Probst, Susanne, Baars, Marieke J.H, Bauer, Ulrike, Pickardt, Thomas, Sperling, Silke R, Berger, Felix, Moorman, Antoon F.M, Mulder, Barbara J.M, Thierfelder, Ludwig, Keavney, Bernard, Goodship, Judith, Klaassen, Sabine

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