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...
| المؤلفون الرئيسيون: | , , , , , , , |
|---|---|
| التنسيق: | Journal article |
| اللغة: | English |
| منشور في: |
Springer Nature
2017
|