Managing genetic information sharing at family and population level
Author:
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41431-023-01514-6.pdf
Reference14 articles.
1. Tiller JM, Stott A, Finlay K, Boughtwood T, Madelli EO, Horton A, et al. Direct notification by health professionals of relatives at-risk of genetic conditions (with patient consent): views of the Australian public. Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01395-9.
2. White S, Turbitt E, Rogers K, Tucker K, Mcewen A, Best M, et al. A survey of genetic and palliative care health professionals’ views of integrating genetics into palliative care. Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01409-6.
3. Rao ND, King KM, Kaganovsky J, Hassan S, Tsinajinne D, Fullerton SM, et al. Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients. Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01460-3.
4. Klemenzdottir EO, Arnadottir GA, Jensson BO, Jonasdottir A, Katrinardottir H, Fridriksdottir R, et al. A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome. Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01455-0.
5. Parijs I, Brison N, Vancoillie L, Baetens M, Blaumeiser B, Boulanger S, et al. Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles. Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01336-6.
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