An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes
Crossref DOI link:
Update policy: https://doi.org/10.1007/SPRINGER_CROSSMARK_POLICY
Le Quesne Stabej, Polona
Stanescu, Horia C.
Williams, Hywel J.
Funding for this research was provided by:
National Institute for Health Research