Anatomic patterns of conotruncal defects associated with deletion 22q11 (Q73840767)

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scientific article published on 01 January 2001

Language	Label	Description	Also known as
English	Anatomic patterns of conotruncal defects associated with deletion 22q11	scientific article published on 01 January 2001

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339377%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Anatomic patterns of conotruncal defects associated with deletion 22q11 (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11339377%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Bruno Dallapiccola

9

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B Dallapiccola

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7 November 2019

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B Marino

1

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7 November 2019

M C Digilio

2

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7 November 2019

A Toscano

3

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7 November 2019

S Anaclerio

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7 November 2019

A Giannotti

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7 November 2019

C Feltri

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7 November 2019

M A de Ioris

7

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7 November 2019

A Angioni

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7 November 2019

publication date

1 January 2001

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7 November 2019

Genetics in Medicine

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7 November 2019

3

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7 November 2019

1

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7 November 2019

45-48

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7 November 2019

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Cardiac malformations in the velocardiofacial syndrome

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

1 reference

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21 January 2018

Frequency of 22q11 deletions in patients with conotruncal defects

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Di George anomaly with atrioventricular canal

1 reference

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21 January 2018

Transposition of the great arteries associated with deletion of chromosome 22q11

1 reference

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21 January 2018

Tricuspid atresia and 22q11 deletion

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Cervical aortic arch associated with 22q11.2 deletion

1 reference

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21 January 2018

Atrioventricular canal in Down syndrome. Prevalence of associated cardiac malformations compared with patients without Down syndrome

1 reference

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21 January 2018

Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal

1 reference

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21 January 2018

Cardiac malformations in patients with oral-facial-skeletal syndromes: clinical similarities with heterotaxia

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21 January 2018

Holt-Oram syndrome and multiple ventricular septal defects: an association suggesting a possible genetic marker?

1 reference

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21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Tetralogy of Fallot associated with chromosome 22q11 deletion

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Deletion within chromosome 22 is common in patients with absent pulmonary valve syndrome

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Prenatal detection of a tetralogy of Fallot with origin of the left pulmonary artery from the ascending aorta in a familial 22q11 microdeletion

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Truncus Arteriosus Communis Associated With Chromosome 22q11 Deletion

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Severe truncal valve dysplasia: association with DiGeorge syndrome?

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Deletion 22q11 in patients with interrupted aortic arch

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Interrupted right aortic arch in DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Association of interrupted aortic arch with malformations producing reduced blood flow to the fourth aortic arches

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

A Genetic Etiology for Interruption of the Aortic Arch Type B

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200101000-00010

21 January 2018

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

1 reference

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21 January 2018

Microdeletion 22q11 in complex cardiovascular malformations

1 reference

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21 January 2018

Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study

1 reference

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21 January 2018

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

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21 January 2018

Search for 22q11 deletion in non-syndromic conotruncal cardiac defects

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21 January 2018

Chromosome 22q11 microdeletion and isolated conotruncal heart defects

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21 January 2018

Conotruncal heart defects and chromosome 22q11 microdeletion

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Congenital Heart Surgery Nomenclature and Database Project: pulmonary atresia--ventricular septal defect

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21 January 2018

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