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Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
German Competence Network for Congenital Heart Defects, Oct 2021, In: Genetics in medicine. 23, 10, p. 1952-1960 9 p.Research output: Contribution to journal › Article* › Academic › peer-review
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Prognostic Value of Maximal and Submaximal Exercise Performance in Fontan Patients < 15 Years of Age
Terol Espinosa de los Monteros, C., Harteveld, L. M., Kuipers, I. M., Rammeloo, L., Hazekamp, M. G., Blom, N. A. & ten Harkel, A. D. J., 1 Sept 2021, In: American journal of cardiology. 154, p. 92-98 7 p.Research output: Contribution to journal › Article* › Academic › peer-review
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Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous case: A heterozygous and a homozygous case
Bruyndonckx, L., Vogelzang, J. L., Bugiani, M., Straver, B., Kuipers, I. M., Onland, W., Nannenberg, E. A., Clur, S.-A. & & van der Crabben, S. N., Aug 2021, In: American journal of medical genetics. Part A. 185, 8, p. 2464-2470 7 p.Research output: Contribution to journal › Article* › Academic › peer-review
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