📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Genetic modifiers in rare disorders: the case of fragile X syndrome. (2021)

First Author: Crawford H

Attributed to: Integrating innovative technologies for genotyping and phenotyping in stratified medicine funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41431-020-00711-x

PubMed Identifier: 32862204

Publication URI: http://europepmc.org/abstract/MED/32862204

Type: Journal Article/Review

Volume: 29

Parent Publication: European journal of human genetics : EJHG

Issue: 1

ISSN: 1018-4813