Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome
about
Embryonic aortic arch hemodynamics are a functional biomarker for ethanol-induced congenital heart defects [Invited]Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease.Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndromeGenetic counseling in the adult with congenital heart disease: what is the role?Tetralogy of Fallot: epidemiology meets real-world management: lessons from the Baltimore-Washington Infant Study.Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling.Transgenerational cardiology: One way to a baby's heart is through the mother.Prenatal diagnosis of a 22q11 deletion in a second-trimester fetus with conotruncal anomaly, absent thymus and meningomyelocele: Kousseff syndrome.Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.
P2860
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P2860
Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome
description
2009 nî lūn-bûn
@nan
2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome
@ast
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome
@en
type
label
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome
@ast
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome
@en
prefLabel
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome
@ast
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome
@en
P2093
P2860
P356
P1476
Evaluation of potential modifi ...... the 22q11.2 deletion syndrome
@en
P2093
Beverly S Emanuel
Deborah A Driscoll
Elizabeth Goldmuntz
Laura E Mitchell
Minghua Mei
P2860
P304
P356
10.1002/BDRA.20501
P577
2009-02-01T00:00:00Z