In a medical first, 100,000 newborns in England will have their entire genomes sequenced in order to detect and treat rare genetic diseases as early as possible. JaneDJourno reports.
The government-funded study – which will take place over the next two years – is designed to gauge the health and cost benefits of decoding the DNA of healthy babies. If successful, it could be rolled out nationwide.
Belgique Dernières Nouvelles, Belgique Actualités
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