Tetralogy of Fallot associated with chromosome 22q11 deletion (Q72064736)

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scientific article published on September 15, 1995

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Language	Label	Description	Also known as
English	Tetralogy of Fallot associated with chromosome 22q11 deletion	scientific article published on September 15, 1995

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7677092%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

title

Tetralogy of Fallot associated with chromosome 22q11 deletion (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7677092%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

main subject

tetralogy of Fallot

1 reference

based on heuristic

inferred from title

human chromosome 22

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7677092

retrieved

9 August 2024

chromosomal deletion syndrome

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7677092

retrieved

9 August 2024

author name string

K. Momma

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7677092

retrieved

9 August 2024

C. Kondo

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7677092

retrieved

9 August 2024

M. Ando

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7677092

retrieved

9 August 2024

R. Matsuoka

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7677092

retrieved

9 August 2024

A. Takao

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7677092

retrieved

9 August 2024

language of work or name

English

0 references

publication date

1 September 1995

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7677092%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

15 September 1995

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

7677092

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7677092

retrieved

9 August 2024

full work available at URL

https://api.elsevier.com/content/article/PII:S0002914999801702?httpAccept=text/xml

1 reference

stated in

Crossref

DOI

10.1016/S0002-9149(99)80170-2

reference URL

https://api.crossref.org/works/10.1016/S0002-9149(99)80170-2

retrieved

9 August 2024

https://api.elsevier.com/content/article/PII:S0002914999801702?httpAccept=text/plain

1 reference

stated in

Crossref

DOI

10.1016/S0002-9149(99)80170-2

reference URL

https://api.crossref.org/works/10.1016/S0002-9149(99)80170-2

retrieved

9 August 2024

published in

American Journal of Cardiology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7677092%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

volume

76

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7677092%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

issue

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7677092%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

page(s)

618-621

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7677092%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

cites work

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2980170-2

retrieved

7 January 2021

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2980170-2

retrieved

7 January 2021

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2980170-2

retrieved

7 January 2021

DiGeorge syndrome: part of CATCH 22.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2980170-2

retrieved

7 January 2021

Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2980170-2

retrieved

7 January 2021

Role of neural crest in congenital heart disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0002-9149%2899%2980170-2

retrieved

7 January 2021

Identifiers

DOI

10.1016/S0002-9149(99)80170-2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7677092%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

PubMed publication ID

7677092

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7677092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7677092%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 October 2019

 

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