Clinical genomics testing: mainstreaming and globalising
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/s41431-022-01131-9.pdf
Reference11 articles.
1. Slomp C, Morris E, GenCOUNSEL Study, Price M, Elliott AM, Austin J. The stepwise process of integrating a genetic counsellor into primary care. Eur J Hum Genet. 2022. https://doi.org/10.1038/s41431-022-01040-x
2. van Vliet ME, Kerkhoffs JH, Harteveld CL, Houwink EJF. Hemoglobinopathy prevention in primary care: a reflection of underdetection and difficulties with accessibility of medical care, a quantitative study. Eur J Hum Genet. 2022. https://doi.org/10.1038/s41431-022-01051-8
3. Phillips A, Bronselaer T, Borry P, Van Hoyweghen I, Vears DF, Pasquier L, et al. Informing relatives of their genetic risk: an examination of the Belgian legal context. Eur J Hum Genet. 2022. https://doi.org/10.1038/s41431-021-01016-3
4. Ormondroyd E, Border P, Hayward J, Papanikitas A. Genomic health data generation in the UK: a 360 view. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00976-w
5. Evans DG, Mostaccioli S, Pang D, Fadzil O, Connor M, Pittara M, et al. ERN GENTURIS clinical practice guidelines for the diagnosis, treatment, management and surveillance of people with schwannomatosis. Eur J Hum Genet. 2022. https://doi.org/10.1038/s41431-022-01086-x
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