Paediatric genomics: diagnosing rare disease in children
Paediatric genomics: diagnosing rare disease in children, Published online: 05 February 2018; doi:10.1038/nrg.2017.116
The emerging field of paediatric genomics has leveraged the power of next-generation sequencing technologies to improve the diagnostic rates of rare disease in children. This Review addresses key considerations for safe and effective implementation of genomics in the clinic.
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