Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome. (2020)
Attributed to:
From Microcephaly to Genome Stability,
Inflammation and Growth Regulation
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2019-106396
PubMed Identifier: 31784481
Publication URI: http://europepmc.org/abstract/MED/31784481
Type: Journal Article/Review
Volume: 57
Parent Publication: Journal of medical genetics
Issue: 3
ISSN: 0022-2593