Why don’t we all use genomic testing?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/s41431-023-01446-1.pdf
Reference13 articles.
1. Mordaunt DA, Dalziel K, Goranitis I, Stark Z. Uptake of funded genomic testing for syndromic and non-syndromic intellectual disability in Australia. Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01417-6.
2. Strnadová I, Loblinzk J, Scully JL, Danker J, Tso M, Jackaman K-M, et al. “I am not a number!” Opinions and preferences of people with intellectual disability about genetic healthcare. Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01282-3.
3. Ballard LM, Band R, Lucassen AM. Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM). Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01400-1.
4. Oexle K, Zech M, Stühn LG, Siegert S, Brunet T, Schmidt WM, et al. Episignature analysis of moderate effects and mosaics. Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01406-9.
5. Lee S, Ochoa E, Badura-Stronka M, Donnelly D, Lederer D, Lynch SA, et al. Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome. Eur J Hum Genet. 2023. https://doi.org/10.1038/s41431-023-01422-9.
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