Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing. (2022)

First Author: Macken WL
Attributed to:  UK Infrastructure for Large-scale Clinical Genomics Research funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41467-022-32908-7

PubMed Identifier: 36344503

Publication URI: http://europepmc.org/abstract/MED/36344503

Type: Journal Article/Review

Volume: 13

Parent Publication: Nature communications

Issue: 1

ISSN: 2041-1723