Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia. (2023)

First Author: Hall HN
Attributed to:  Developmental Disorders: From Diagnosis to Mechanism via Cis-Regulation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmg-2023-109181

PubMed Identifier: 38050128

Publication URI: http://europepmc.org/abstract/MED/38050128

Type: Journal Article/Review

Parent Publication: Journal of medical genetics

ISSN: 0022-2593