Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study
Whole-exome/whole-genome sequencing (WES/WGS) has the potential to enhance genetic diagnosis of rare disease, and is increasingly becoming part of routine clinical care in mainstream medicine. Effective translation will require ongoing efforts in a number of areas including: selection of appropriate...
Những tác giả chính: | Ormondroyd, E, Mackley, M, Blair, E, Craft, J, Knight, J, Taylor, J, Wilkie, A, Watkins, H |
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Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
Springer Nature
2017
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