(Q58141926)

English

Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery

scientific article published on 03 January 2008

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

circulatory system

1 reference

based on heuristic

inferred from title

Lidia Ziółkowska

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Anna Turska-Kmieć

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Małgorzata Krajewska-Walasek

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Bohdan Maruszewski

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Piotr Burczyński

8

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Grażyna Brzezińska-Rajszys

5

object named as

Grazyna Brzezinska-Rajszys

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

2

object named as

Wanda Kawalec

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

author name string

Jadwiga Daszkowska

6

1 reference

Europe PubMed Central

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31 December 2019

publication date

3 January 2008

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Europe PubMed Central

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31 December 2019

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

167

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

10

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Europe PubMed Central

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31 December 2019

1135-1140

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

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

1 reference

https://api.crossref.org/works/10.1007%2FS00431-007-0645-2

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Results of a policy of primary repair of truncus arteriosus in the neonate

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anatomic patterns of conotruncal defects associated with deletion 22q11

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities in lymphocyte populations in infants with neural crest cardiovascular defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Operative mortality and frequency of coexistent anomalies in interruption of the aortic arch

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of 22q11 deletions in patients with conotruncal defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Management strategy and long-term outcome for truncus arteriosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Philadelphia story: the 22q11.2 deletion: report on 250 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tetralogy of Fallot associated with chromosome 22q11 deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac malformations in the velocardiofacial syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Truncus arteriosus communis associated with chromosome 22q11 deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/18172682

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-007-0645-2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18172682%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

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