Conotruncal heart defects and chromosome 22q11 microdeletion (Q73236494)

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scientific article published on 01 April 1997

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Language	Label	Description	Also known as
English	Conotruncal heart defects and chromosome 22q11 microdeletion	scientific article published on 01 April 1997

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

title

Conotruncal heart defects and chromosome 22q11 microdeletion (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

author

Bruno Dallapiccola

series ordinal

5

object named as

B Dallapiccola

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

author name string

M C Digilio

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

B Marino

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

A Giannotti

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

G Novelli

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

language of work or name

English

0 references

publication date

1 April 1997

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

published in

The Journal of Pediatrics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

volume

130

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

page(s)

675-677

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

cites work

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

Chromosome 22q11 monosomy and the genetic basis of congenital heart disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

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

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970260-9

retrieved

7 January 2021

Identifiers

DOI

10.1016/S0022-3476(97)70260-9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

PubMed publication ID

9108874

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9108874

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9108874%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

 

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