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Genetic diagnosis for rare diseases in the Dutch Caribbean: a qualitative study on the experiences and associated needs of parents.
Verberne EA, van den Heuvel LM, Ponson-Wever M, de Vroomen M, Manshande ME, Faries S, Ecury-Goossen GM, Henneman L, van Haelst MM. Verberne EA, et al. Among authors: van den heuvel lm. Eur J Hum Genet. 2022 May;30(5):587-594. doi: 10.1038/s41431-022-01039-4. Epub 2022 Jan 28. Eur J Hum Genet. 2022. PMID: 35087185 Free PMC article.
Societal implications of expanded universal carrier screening: a scoping review.
van den Heuvel LM, van den Berg N, Janssens ACJW, Birnie E, Henneman L, Dondorp WJ, Plantinga M, van Langen IM. van den Heuvel LM, et al. Eur J Hum Genet. 2023 Jan;31(1):55-72. doi: 10.1038/s41431-022-01178-8. Epub 2022 Sep 12. Eur J Hum Genet. 2023. PMID: 36097155 Free PMC article. Review.
Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counselees.
van den Heuvel LM, Huisinga MJ, Hoedemaekers YM, Baas AF, Plantinga M, Henneman L, van Tintelen JP, Smets EMA, Christiaans I. van den Heuvel LM, et al. Among authors: van tintelen jp. Eur J Hum Genet. 2019 Sep;27(9):1341-1350. doi: 10.1038/s41431-019-0410-9. Epub 2019 May 3. Eur J Hum Genet. 2019. PMID: 31053782 Free PMC article.
Long-Term Follow-Up Study on the Uptake of Genetic Counseling and Predictive DNA Testing in Inherited Cardiac Conditions.
van den Heuvel LM, van Teijlingen MO, van der Roest W, van Langen IM, Smets EMA, van Tintelen JP, Christiaans I. van den Heuvel LM, et al. Among authors: van der roest w, van langen im, van teijlingen mo, van tintelen jp. Circ Genom Precis Med. 2020 Oct;13(5):524-530. doi: 10.1161/CIRCGEN.119.002803. Epub 2020 Aug 14. Circ Genom Precis Med. 2020. PMID: 33079600 Free PMC article.
23 results