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