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Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships
Lauffer, P., Pals, G., Zwinderman, A. H., Postema, F. A. M., Baars, M. J. H., Dulfer, E., Hilhorst-Hofstee, Y., Houweling, A. C., Kempers, M., Krapels, I. P. C., van de Laar, I. M. B. H., Loeys, B., Spaans, A. M. J., Warnink-Kavelaars, J., de Waard, V., Wit, J. M. & Menke, L. A., Nov 2022, In: American Journal of Medical Genetics. Part A. n/a, n/aResearch output: Contribution to Journal › Article › Academic › peer-review
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A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial
van den Heuvel, L. M., Hoedemaekers, Y. M., Baas, A. F., Baars, M. J. H., van Tintelen, J. P., Smets, E. M. A. & Christiaans, I., 24 Nov 2021, (E-pub ahead of print) In: European journal of human genetics.Research output: Contribution to Journal › Article › Academic › peer-review
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Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient
Marsili, L., Overwater, E., Hanna, N., Baujat, G., Baars, M. J. H., Boileau, C., Bonneau, D., Brehin, A. C., Capri, Y., Cheung, H. Y., Dulfer, E., Gerard, M., Gouya, L., Hilhorst-Hofstee, Y., Houweling, A. C., Isidor, B., Le Gloan, L., Menke, L. A., Odent, S., Morice-Picard, F., & 5 others, 1 May 2020, In: Clinical genetics. 97, 5, p. 723-730 8 p.Research output: Contribution to Journal › Article › Academic › peer-review
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