Using high-resolution variant frequencies to empower clinical genome interpretation. (2017)

First Author: Whiffin N

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/gim.2017.26

PubMed Identifier: 28518168

Publication URI: http://europepmc.org/abstract/MED/28518168

Type: Journal Article/Review

Volume: 19

Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics

Issue: 10

ISSN: 1098-3600