(Q81376555)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17906889%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

The fate of children with microdeletion 22q11.2 syndrome and congenital heart defect: clinical course and cardiac outcome (English)

1 reference

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8 January 2020

4

1 reference

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8 January 2020

author name string

A Kyburz

1

1 reference

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8 January 2020

U Bauersfeld

2

1 reference

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8 January 2020

A Schinzel

3

1 reference

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8 January 2020

M Hug

5

1 reference

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8 January 2020

M Tomaske

6

1 reference

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8 January 2020

E R Valsangiacomo Büchel

7

1 reference

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8 January 2020

publication date

29 September 2007

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8 January 2020

1 reference

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8 January 2020

volume

29

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8 January 2020

issue

1

1 reference

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8 January 2020

page(s)

76-83

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https://scigraph.springernature.com/pub.10.1007/s00246-007-9074-2

8 January 2020

exact match

0 references

cites work

Influence of chromosome 22q11.2 microdeletion on surgical outcome after treatment of tetralogy of fallot with pulmonary atresia

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12 December 2020

A cohort study of neurodevelopmental outcome in children with DiGeorge syndrome following cardiac surgery

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12 December 2020

Long-term Results after Repair of Truncus Arteriosus Communis in Neonates and Infants

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12 December 2020

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

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12 December 2020

Anatomic patterns of conotruncal defects associated with deletion 22q11

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12 December 2020

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

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12 December 2020

Guidelines for 22q11 deletion screening of patients with conotruncal defects

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12 December 2020

Truncus arteriosus repair: outcomes, risk factors, reoperation and management

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12 December 2020

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

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12 December 2020

Aortic Arch Anomalies Associated with Chromosome 22q11 Deletion (CATCH 22)

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12 December 2020

22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin

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12 December 2020

Clinical features of 78 adults with 22q11 Deletion Syndrome.

1 reference

12 December 2020

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

1 reference

12 December 2020

Repair of interrupted aortic arch: a ten-year experience

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12 December 2020

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

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12 December 2020

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

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12 December 2020

Early and long-term results of the surgical treatment of tetralogy of Fallot with pulmonary atresia, with or without major aortopulmonary collateral arteries

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12 December 2020

Conotruncal heart defects: impact of genetic syndromes on immediate operative mortality

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12 December 2020

Assessment of the thymus at echocardiography in fetuses at risk for 22q11.2 deletion

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12 December 2020

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

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A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

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12 December 2020

Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults

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12 December 2020

Genetic Syndromes and Outcome After Surgical Correction of Tetralogy of Fallot

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12 December 2020

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

1 reference

12 December 2020

Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk.

1 reference

12 December 2020

Presenting phenotype in 100 children with the 22q11 deletion syndrome.

1 reference

12 December 2020

The influence of pulmonary artery morphology on the results of operations for major aortopulmonary collateral arteries and complex congenital heart defects

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12 December 2020

Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q11.2 deletion.

1 reference

12 December 2020

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

1 reference

12 December 2020