Assessment of the incorporation of CNV surveillance into gene panel next-generation sequencing testing for inherited retinal diseases. (2018)

First Author: Ellingford JM

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2017-104791

PubMed Identifier: 29074561

Publication URI: http://europepmc.org/abstract/MED/29074561

Type: Journal Article/Review

Volume: 55

Parent Publication: Journal of medical genetics

Issue: 2

ISSN: 0022-2593