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A framework for reporting secondary and incidental findings in prenatal sequencing: When and for whom?
As the use of genomic sequencing (GS) in the prenatal setting becomes more widespread, laboratories and clinicians will be tasked with making decisions about whether to offer incidental and secondary findings to expectant parents and, if so, which ones. Unfortunately, few guidelines or position stat...
Autores principales: | Vears, Danya, Amor, David J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306573/ https://www.ncbi.nlm.nih.gov/pubmed/35032068 http://dx.doi.org/10.1002/pd.6097 |
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