📣 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.

Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study. (2015)

First Author: Luciano M

Attributed to: Elucidating the mechanism by which the SHROOM2 locus on Xp22.2 contributes to colorectal cancer aetiology. funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1017/thg.2015.10

PubMed Identifier: 25744449

Publication URI: http://europepmc.org/abstract/MED/25744449

Type: Journal Article/Review

Volume: 18

Parent Publication: Twin research and human genetics : the official journal of the International Society for Twin Studies

Issue: 2

ISSN: 1832-4274