1
Copier, Jaël S., Bootsma, Marianne, Ng, Chai A., Wilde, Arthur A. M., Bertels, Robin A., Bikker, Hennie, Christiaans, Imke, van der Crabben, Saskia N., Hol, Janna A., Koopmann, Tamara T., Knijnenburg, Jeroen, Lommerse, Aafke A. J., van der Smagt, Jasper J., Bezzina, Connie R., Vandenberg, Jamie I., Verkerk, Arie O., Barge-Schaapveld, Daniela Q. C. M., Lodder, Elisabeth M.
Veröffentlicht in: Copier , J S , Bootsma , M , Ng , C A , Wilde , A A M , Bertels , R A , Bikker , H , Christiaans , I , van der Crabben , S N , Hol , J A , Koopmann , T T , Knijnenburg , J , Lommerse , A A J , van der Smagt , J J , Bezzina , C R , Vandenberg , J I , Verkerk , A O , Barge-Schaapveld , D Q C M & Lodder , E M 2023 , ' Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance ' , Human Molecular Genetics , vol. 32 , no. 7 , pp. 1072-1082 . https://doi.org/10.1093/hmg/ddac261;
2023
Veröffentlicht in: Copier , J S , Bootsma , M , Ng , C A , Wilde , A A M , Bertels , R A , Bikker , H , Christiaans , I , van der Crabben , S N , Hol , J A , Koopmann , T T , Knijnenburg , J , Lommerse , A A J , van der Smagt , J J , Bezzina , C R , Vandenberg , J I , Verkerk , A O , Barge-Schaapveld , D Q C M & Lodder , E M 2023 , ' Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance ' , Human Molecular Genetics , vol. 32 , no. 7 , pp. 1072-1082 . https://doi.org/10.1093/hmg/ddac261;
2023
2
Cox, Moniek G. P. J., van der Zwaag, Paul A., van der Werf, Christian, van der Smagt, Jasper J., Noorman, Maartje, Bhuiyan, Zahir A., Wiesfeld, Ans C. P., Volders, Paul G. A., van Langen, Irene M., Atsma, Douwe E., Dooijes, Dennis, van den Wijngaard, Arthur, Houweling, Arjan C., Jongbloed, Jan D. H., Jordaens, Luc J. L. M., Cramer, Maarten Jan, Doevendans, Pieter A., de Bakker, Jacques M. T., Wilde, Arthur A. M., van Tintelen, J. Peter, Hauer, Richard N. W.
Veröffentlicht in: Cox , M G P J , van der Zwaag , P A , van der Werf , C , van der Smagt , J J , Noorman , M , Bhuiyan , Z A , Wiesfeld , A C P , Volders , P G A , van Langen , I M , Atsma , D E , Dooijes , D , van den Wijngaard , A , Houweling , A C , Jongbloed , J D H , Jordaens , L J L M , Cramer , M J , Doevendans , P A , de Bakker , J M T , Wilde , A A M , van Tintelen , J P & Hauer , R N W 2011 , ' Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Pathogenic Desmosome Mutations in Index-Patients Predict Outcome of Family Screening: Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Genotype-Phenotype Follow-Up Study ' , Circulation , vol. 123 , no. 23 , pp. 2690-2700 . https://doi.org/10.1161/CIRCULATIONAHA.110.988287;
2011
Veröffentlicht in: Cox , M G P J , van der Zwaag , P A , van der Werf , C , van der Smagt , J J , Noorman , M , Bhuiyan , Z A , Wiesfeld , A C P , Volders , P G A , van Langen , I M , Atsma , D E , Dooijes , D , van den Wijngaard , A , Houweling , A C , Jongbloed , J D H , Jordaens , L J L M , Cramer , M J , Doevendans , P A , de Bakker , J M T , Wilde , A A M , van Tintelen , J P & Hauer , R N W 2011 , ' Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Pathogenic Desmosome Mutations in Index-Patients Predict Outcome of Family Screening: Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Genotype-Phenotype Follow-Up Study ' , Circulation , vol. 123 , no. 23 , pp. 2690-2700 . https://doi.org/10.1161/CIRCULATIONAHA.110.988287;
2011