about
Survival among children with "Lethal" congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN).Arthrogryposis multiplex congenita in utero: radiologic and pathologic findings.The multiple faces of TOR1A: different inheritance, different phenotype.Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type.
P2860
description
2016 nî lūn-bûn
@nan
2016 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@ast
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@en
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@nl
type
label
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@ast
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@en
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@nl
prefLabel
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@ast
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@en
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@nl
P2860
P356
P1476
Arthrogryposis as a Syndrome: Gene Ontology Analysis
@en
P2093
Jeff Kiefer
P2860
P356
10.1159/000446617
P407
P577
2016-07-01T00:00:00Z