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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...
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Pubblicato in: | Eur J Hum Genet |
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Autori principali: | , , , , , , , , |
Natura: | Artigo |
Lingua: | Inglês |
Pubblicazione: |
Nature Publishing Group
2017
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Soggetti: | |
Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5427178/ https://ncbi.nlm.nih.gov/pubmed/28327571 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2017.37 |
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