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Wide disparity of clinical genetics services and EU rare disease research funding across Europe
The origins of clinical genetics services vary throughout Europe with some emerging from paediatric medicine and others from an academic laboratory setting. In 2011, the cross-border patients’ rights directive recommended the creation of European Research Networks (ERNs) to improve patient care thro...
Gespeichert in:
| Veröffentlicht in: | J Community Genet |
|---|---|
| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Springer Berlin Heidelberg
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4796048/ https://ncbi.nlm.nih.gov/pubmed/26536881 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12687-015-0256-y |
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