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Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. (2018)

First Author: Gregson CL

Attributed to: Mendelian randomization to hypothesis-free causal inference funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.bone.2018.06.001

PubMed Identifier: 29883787

Publication URI: http://europepmc.org/abstract/MED/29883787

Type: Journal Article/Review

Volume: 114

Parent Publication: Bone

ISSN: 1873-2763