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.from Genetics via xlomafota13 on Inoreader http://ift.tt/2ECUwoJ
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