UK's NHS and Genomics England to use genome sequencing to identify rare diseases in babies
wionews.com
UK's NHS and Genomics England to use genome sequencing to identify rare diseases in babies
Professor Matt Brown, the Chief Scientific Officer at Genomics England has predicted that very soon parents will be able to have it checked if their baby is at a higher risk of illnesses. He said that for this, parents could have their childrenâ s genetic code read by the NHS
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