100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. (2021)

First Author: 100,000 Genomes Project Pilot Investigators
Attributed to:  ISCF HDRUK DIH Sprint Exemplar: Cloud-based integration of phenotype and genotype data for rare disease research funded by ISCF

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1056/nejmoa2035790

PubMed Identifier: 34758253

Publication URI: http://europepmc.org/abstract/MED/34758253

Type: Journal Article/Review

Volume: 385

Parent Publication: The New England journal of medicine

Issue: 20

ISSN: 0028-4793