Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect (Q43661765)

25 November 2017

title

Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect (English)

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25 November 2017

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William T Mahle

1

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25 November 2017

Joseph Crisalli

2

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25 November 2017

Karlene Coleman

3

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25 November 2017

Robert M Campbell

4

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25 November 2017

Vincent K H Tam

5

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25 November 2017

Robert N Vincent

6

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25 November 2017

Kirk R Kanter

7

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25 November 2017

language of work or name

English

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publication date

1 August 2003

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The Annals of Thoracic Surgery

25 November 2017

published in

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25 November 2017

volume

76

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25 November 2017

issue

2

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25 November 2017

page(s)

567-571

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Frequency of 22q11 deletions in patients with conotruncal defects

25 November 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.

7 January 2021

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Congenital cardiac anomalies associated with the DiGeorge syndrome: a neonatal experience

7 January 2021

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Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Total repair of pulmonary atresia with ventricular septal defect and major aortopulmonary collaterals: an integrated approach

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Clinical relevance of monosomy 22q11.2 in children with pulmonary atresia and ventricular septal defect

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Chromosome 22q11 microdeletions in tetralogy of Fallot

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Outcome of pulmonary atresia and ventricular septal defect during infancy

7 January 2021

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Natural and unnatural history of pulmonary atresia

7 January 2021

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Associated cardiac anomalies in isolated and syndromic patients with tetralogy of Fallot.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion

7 January 2021

1 reference

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One-stage midline unifocalization and complete repair in infancy versus multiple-stage unifocalization followed by repair for complex heart disease with major aortopulmonary collaterals

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Early and intermediate outcomes after repair of pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries: experience with 85 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

DiGeorge anomaly: a comparative study of the clinical and immunologic characteristics of patients positive and negative by fluorescence in situ hybridization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-4975%2803%2900516-2

10.1016/S0003-4975(03)00516-2

7 January 2021

Identifiers

DOI

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25 November 2017

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