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flag 100,000 English newborns to be screened for 200 genetic disorders using whole genome sequencing.

flag The NHS in England is launching a pioneering initiative to screen 100,000 newborns for over 200 genetic disorders using whole genome sequencing. flag This program aims to enhance early diagnosis and treatment, potentially transforming outcomes for affected infants. flag Blood samples from umbilical cords will be analyzed to identify conditions that can be treated before symptoms arise. flag The pilot, set to expand to 40 hospitals, represents a significant advancement in newborn healthcare.

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