about
Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.Understanding craniosynostosis as a growth disorderThe molecular and cellular basis of Apert syndrome.Choanal Atresia and Craniosynostosis: Development and Disease.Soluble form of FGFR2 with S252W partially prevents craniosynostosis of the apert mouse model.Research advances in Apert syndrome
P2860
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh-hant
name
Mouse models of Apert syndrome.
@en
Mouse models of Apert syndrome.
@nl
type
label
Mouse models of Apert syndrome.
@en
Mouse models of Apert syndrome.
@nl
prefLabel
Mouse models of Apert syndrome.
@en
Mouse models of Apert syndrome.
@nl
P2860
P1476
Mouse models of Apert syndrome.
@en
P2093
Greg Holmes
P2860
P2888
P304
P356
10.1007/S00381-012-1872-Z
P577
2012-08-08T00:00:00Z