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How whole genome sequencing is revolutionising the rare disease patient experience

Published: June 10, 2022

- PMLiVE

Source: pmlive.com

Related Topics:

United KingdomDisease Diagnosis In Health CareNational Human Genome Research InstituteNewborn Genomes ProgrammeHuman Genome ProjectKingdom BiobankUnited Kingdom BiobankHuman Genome ResearchHuman GenomeAccessed MayProject PilotRare Disease DiagnosisHealth CareAccessed JuneWhole Genome SequencingNewborn Genomes Programme ContinuingGenomics EnglandPublished May