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Opt‐in for secondary findings as part of diagnostic whole‐exome sequencing: Real‐life experience from an international diagnostic laboratory
BACKGROUND: Discussion about the risks and benefits of offering secondary findings as part of genome‐wide diagnostics lacks real‐life data. We studied the opt‐in decisions of patients/families referred to whole exome study (WES) in Blueprint Genetics (BpG), a genetic testing company with customers i...
Autores principales: | Brunfeldt, Minna, Kaare, Milja, Saarinen, Inka, Koskenvuo, Juha, Kääriäinen, Helena |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422066/ https://www.ncbi.nlm.nih.gov/pubmed/37025058 http://dx.doi.org/10.1002/mgg3.2180 |
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