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- W2135028502 endingPage "176" @default.
- W2135028502 startingPage "166" @default.
- W2135028502 abstract "This paper summarizes the current controversies surrounding the identification and disclosure of incidental or secondary findings from genomic sequencing and the implications for genetic counseling practice. The rapid expansion of clinical sequencing has influenced the ascertainment and return of incidental findings, while empiric data to inform best practices are still being generated. Using the North Carolina Clinical Genomic Evaluation by Next Generation Exome Sequencing (NCGENES) research project as an example, we discuss the implications of different models of consent and their impact on patient decisions." @default.
- W2135028502 created "2016-06-24" @default.
- W2135028502 creator A5028470777 @default.
- W2135028502 creator A5068354576 @default.
- W2135028502 date "2015-08-25" @default.
- W2135028502 modified "2023-09-27" @default.
- W2135028502 title "Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice" @default.
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- W2135028502 doi "https://doi.org/10.1007/s40142-015-0075-9" @default.
- W2135028502 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4633435" @default.