Publication
Title
Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosis
Author
Abstract
Language
English
Source (journal)
Bone / International Bone and Mineral Society. - New York
Publication
New York : 2013
ISSN
8756-3282
Volume/pages
52:1(2013), p. 292-295
ISI
000312750700034
Full text (Publisher's DOI)
Full text (publisher's version - intranet only)
UAntwerpen
Faculty/Department
Research group
Project info
Molecular genetic and functional analysis of the role of Wnt signaling in the pathogenesis of osteoporosis and obesity.
Application of whole exome sequencing to identify the genetic defect in hereditary connective tissue disorders
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 15.02.2013
Last edited 08.11.2019
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