A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.
about
A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.
description
1997 nî lūn-bûn
@nan
1997 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
A novel mutation (a886g) in ex ...... n phenotype and plagiocephaly.
@ast
A novel mutation (a886g) in ex ...... n phenotype and plagiocephaly.
@en
type
label
A novel mutation (a886g) in ex ...... n phenotype and plagiocephaly.
@ast
A novel mutation (a886g) in ex ...... n phenotype and plagiocephaly.
@en
prefLabel
A novel mutation (a886g) in ex ...... n phenotype and plagiocephaly.
@ast
A novel mutation (a886g) in ex ...... n phenotype and plagiocephaly.
@en
P2093
P2860
P356
P1476
A novel mutation (a886g) in ex ...... n phenotype and plagiocephaly.
@en
P2093
Collmann H
Schmalenberger B
Steinberger D
P2860
P304
P356
10.1136/JMG.34.5.420
P407
P577
1997-05-01T00:00:00Z