Published in

Elsevier, Genetics in Medicine, 1(20), p. 159-163, 2018

DOI: 10.1038/gim.2017.86

Links

Tools

Export citation

Search in Google Scholar

Long-read genome sequencing identifies causal structural variation in a Mendelian disease

This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
Red circle
Postprint: archiving forbidden
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO