A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
about
The Fibroblast Growth Factor signaling pathwayExpanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants.Apert syndrome with S252W FGFR2 mutation and characterization using Phenomizer: An Indian case report.Mouse models of Apert syndrome.FGFR-associated craniosynostosis syndromes and gastrointestinal defects.Research advances in Apert syndrome
P2860
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
description
2011 nî lūn-bûn
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2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
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2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年论文
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name
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@ast
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@en
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@nl
type
label
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@ast
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@en
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@nl
prefLabel
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@ast
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@en
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@nl
P2860
P356
P1433
P1476
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
@en
P2093
Regan E M Klatt
Sarah C Bowdin
P2860
P2888
P356
10.1186/1471-2350-12-122
P577
2011-09-23T00:00:00Z
P5875
P6179
1035623511