Edit search
Heterozygous mutations of FREM1 are associated with an incre…
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
Article, Chapter
Authors: L.E.L.M. Vissers
Publication: PLoS Genetics, Volume:7, Issue:9, Page(s):e1002278-e1002278
Published: Public Library of Science, 2011
ISSN: 1553-7390
  Full text availability for this item
Browse related articles
  Print copies at your library
  Request a copy of this item
Cite this item