(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

author name string

B Marino

1

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

2

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

3

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

4

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

5

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

6

1 reference

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7 November 2019

M A de Ioris

7

1 reference

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7 November 2019

A Angioni

8

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

9

1 reference

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7 November 2019

publication date

1 January 2001

1 reference

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7 November 2019

1 reference

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7 November 2019

volume

3

1 reference

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7 November 2019

issue

1

1 reference

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7 November 2019

page(s)

45-48

1 reference

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https://scigraph.springernature.com/pub.10.1097/00125817-200101000-00010

7 November 2019

exact match

0 references

cites work

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Cardiac malformations in the velocardiofacial syndrome

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Frequency of 22q11 deletions in patients with conotruncal defects

21 January 2018

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Di George anomaly with atrioventricular canal

21 January 2018

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

21 January 2018

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Tricuspid atresia and 22q11 deletion

21 January 2018

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Cervical aortic arch associated with 22q11.2 deletion

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Tetralogy of Fallot associated with chromosome 22q11 deletion

21 January 2018

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

21 January 2018

1 reference

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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

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

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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Truncus arteriosus communis associated with chromosome 22q11 deletion

21 January 2018

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Severe truncal valve dysplasia: association with DiGeorge syndrome?

21 January 2018

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Deletion 22q11 in patients with interrupted aortic arch

21 January 2018

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Interrupted right aortic arch in DiGeorge syndrome

21 January 2018

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

21 January 2018

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21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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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

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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