Common skeletal features in rare diseases: New links between ciliopathies and FGF-related syndromes. (2013)

First Author: Yannakoudakis BZ
Attributed to:  Small molecule control of Wnt signal transduction funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.4161/rdis.27109

PubMed Identifier: 25003013

Publication URI: http://europepmc.org/abstract/MED/25003013

Type: Journal Article/Review

Volume: 1

Parent Publication: Rare diseases (Austin, Tex.)

ISSN: 2167-5511