Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.
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New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricleGenetics of congenital heart disease: the glass half emptyA human laterality disorder caused by a homozygous deleterious mutation in MMP21Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies.The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease
P2860
Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.
description
2007 nî lūn-bûn
@nan
2007 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@ast
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@en
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@nl
type
label
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@ast
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@en
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@nl
prefLabel
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@ast
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@en
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@nl
P2093
P2860
P1476
Variants of the CFC1 gene in p ...... th congenital cardiac disease.
@en
P2093
Elif Seda Selamet Tierney
Melissa B Rutkin
Wendy K Chung
Zvi Marans
P2860
P304
P356
10.1017/S1047951107000455
P577
2007-04-20T00:00:00Z