-
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
-
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
-
The prognosis of common arterial trunk from a fetal perspective: A prenatal cohort study and systematic literature review: A prenatal cohort study and systematic literature review
van Nisselrooij, A. E. L., Herling, L., Clur, S.-A., Linskens, I. H., Pajkrt, E., Rammeloo, L. A., ten Harkel, A. D. J., Hazekamp, M. G., Blom, N. A. & Haak, M. C., May 2021, In: Prenatal diagnosis. 41, 6, p. 754-765 12 p.Research output: Contribution to journal › Article* › Academic › peer-review
- All publications
