Genomic sequencing in newborn screening: balancing consent with the right of the asymptomatic at-risk child to be found.
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| Title: | Genomic sequencing in newborn screening: balancing consent with the right of the asymptomatic at-risk child to be found. |
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| Authors: | Knoppers BM; Centre of Genomics and Policy, Department of Human Genetics, Faculty of Medicine and Health Sciences, McGill University, Montreal, QC, Canada., Bonilha AE; McGill University Health Centre, Department of Human Genetics, Montreal, QC, Canada., Laberge AM; Medical Genetics, Department of Pediatrics, CHU Sainte-Justine and Université de Montréal, Montreal, QC, Canada., Ahmed A; Our Future Health, London, United Kingdom., Newson AJ; Sydney Health Ethics, Sydney School of Public Health, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. ainsley.newson@sydney.edu.au. |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2025 Mar; Vol. 33 (2), pp. 182-188. Date of Electronic Publication: 2024 Aug 12. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1476-5438 |
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| DOI: | 10.1038/s41431-024-01677-w |
