22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases
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Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart diseaseGenome-wide association study of maternal and inherited loci for conotruncal heart defects.The importance of copy number variation in congenital heart disease22q11.2 Deletion syndrome is associated with increased perioperative events and more complicated postoperative course in infants undergoing infant operative correction of truncus arteriosus communis or interrupted aortic arch22q11.2 deletion status and disease burden in children and adolescents with tetralogy of Fallot.MESP1 Mutations in Patients with Congenital Heart Defects.DGCR6 at the proximal part of the DiGeorge critical region is involved in conotruncal heart defects.22q11.2 deletion syndromeMorbidity in children and adolescents after surgical correction of truncus arteriosus communis.HIRA Gene is Lower Expressed in the Myocardium of Patients with Tetralogy of FallotEffect of 22q11.2 deletion on bleeding and transfusion utilization in children with congenital heart disease undergoing cardiac surgery.Heart failure in congenital heart disease: a confluence of acquired and congenital.The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome.Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.Prevalence of Noncardiac and Genetic Abnormalities in Neonates Undergoing Cardiac Operations: Analysis of The Society of Thoracic Surgeons Congenital Heart Surgery Database.De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients.Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting.Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome.Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.Right aortic arch with isolation of the left subclavian artery: a rare association with airway obstruction.Risk of congenital heart disease in relatives of probands with conotruncal cardiac defects: an evaluation of 1,620 families.22q11.2 Deletion Status and Perioperative Outcomes for Tetralogy of Fallot with Pulmonary Atresia and Multiple Aortopulmonary Collateral Vessels
P2860
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P2860
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases
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2013 nî lūn-bûn
@nan
2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases
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22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases
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type
label
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases
@ast
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases
@en
prefLabel
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases
@ast
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases
@en
P2093
P2860
P1433
P1476
22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases
@en
P2093
Beverly S Emanuel
Elizabeth Goldmuntz
Jennifer Garbarini
Laura E Mitchell
Shabnam Peyvandi
Sharon Edman
Stacy Woyciechowski
P2860
P2888
P304
P356
10.1007/S00246-013-0694-4
P577
2013-04-21T00:00:00Z
P6179
1052440818