Fighting congenital anomalies and rare diseases with information
Posted by:
Christine Harvey, Jem Rashbass and Sarah Stevens, Posted on:
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Categories:
A single knowledge and intelligence service, Chief Knowledge Officer, Reducing preventable deaths
...can also support Genomics England’s 100,000 Genome Project and the significant and important developments in Europe on rare disease registration. Establishing a national Congenital Anomaly and Rare Disease Registration Service...