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

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

7 November 2019

title

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

1 reference

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

7 November 2019

B Dallapiccola

1 reference

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

7 November 2019

B Marino

1 reference

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

7 November 2019

M C Digilio

1 reference

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

7 November 2019

A Toscano

1 reference

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

7 November 2019

S Anaclerio

1 reference

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

7 November 2019

A Giannotti

1 reference

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

7 November 2019

C Feltri

1 reference

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

7 November 2019

M A de Ioris

1 reference

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

7 November 2019

A Angioni

1 reference

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

7 November 2019

publication date

1 January 2001

1 reference

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

7 November 2019

1 reference

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

7 November 2019

volume

1 reference

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

7 November 2019

issue

1 reference

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

7 November 2019

page(s)

45-48

1 reference

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

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

7 November 2019

cites work

1 reference

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

Cardiac malformations in the velocardiofacial syndrome

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Frequency of 22q11 deletions in patients with conotruncal defects

21 January 2018

1 reference

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

Di George anomaly with atrioventricular canal

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Tricuspid atresia and 22q11 deletion

21 January 2018

1 reference

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

Cervical aortic arch associated with 22q11.2 deletion

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Tetralogy of Fallot associated with chromosome 22q11 deletion

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Truncus Arteriosus Communis Associated With Chromosome 22q11 Deletion

21 January 2018

1 reference

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

Severe truncal valve dysplasia: association with DiGeorge syndrome?

21 January 2018

1 reference

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

Deletion 22q11 in patients with interrupted aortic arch

21 January 2018

1 reference

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

Interrupted right aortic arch in DiGeorge syndrome

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

A Genetic Etiology for Interruption of the Aortic Arch Type B

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Microdeletion 22q11 in complex cardiovascular malformations

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Chromosome 22q11 microdeletion and isolated conotruncal heart defects

21 January 2018

1 reference

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

Conotruncal heart defects and chromosome 22q11 microdeletion

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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