Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect. (Q41912446)

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scientific article published on February 1998

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English	Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect.	scientific article published on February 1998

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

title

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

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

main subject

tetralogy of Fallot

1 reference

based on heuristic

inferred from title

author

Stanislas Lyonnet

series ordinal

6

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

author name string

M Chessa

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

G Butera

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

P Bonhoeffer

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

L Iserin

series ordinal

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

J Kachaner

series ordinal

5

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

A Munnich

series ordinal

7

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

D Sidi

series ordinal

8

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

D Bonnet

series ordinal

9

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

language of work or name

English

0 references

publication date

1 February 1998

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stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

published in

Heart

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

volume

79

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

issue

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

page(s)

186-190

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Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

cites work

American College of Cardiology 45th Annual Scientific Session, Orlando, Florida, March 24 to 27, 1996.

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PubMed Central

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5 June 2018

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

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5 June 2018

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

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728608

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5 June 2018

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

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PubMed Central

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5 June 2018

Toward a molecular understanding of congenital heart disease

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5 June 2018

Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome

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5 June 2018

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

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5 June 2018

Cardiovascular malformations in DiGeorge syndrome (congenital absence of hypoplasia of the thymus)

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PubMed Central

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5 June 2018

Neural crest cells contribute to normal aorticopulmonary septation

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728608

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5 June 2018

Mesenchymal derivatives from the neural crest

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728608

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5 June 2018

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

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PubMed Central

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5 June 2018

Dinucleotide repeat polymorphism at the D22S264 locus

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5 June 2018

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

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PubMed Central

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5 June 2018

Development of the pharyngeal arch system related to the pulmonary and bronchial vessels in the avian embryo. With a concept on systemic-pulmonary collateral artery formation.

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18 August 2018

Human haploinsufficiency — one for sorrow, two for joy

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2 December 2018

Microsatellite DNA markers detects 95% of chromosome 22q11 deletions

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9538314

retrieved

12 December 2020

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A new method for the quantitative standardization of cross-sectional areas of the pulmonary arteries in congenital heart diseases with decreased pulmonary blood flow

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9538314

retrieved

12 December 2020

based on heuristic

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Pathogenesis of persistent truncus arteriosus and dextroposed aorta in the chick embryo after neural crest ablation

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9538314

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac morphogenesis--recent research advances

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9538314

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9538314

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The restricted surgical relevance of morphologic criteria to classify systemic-pulmonary collateral arteries in pulmonary atresia with ventricular septal defect

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9538314

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tetralogy of Fallot associated with chromosome 22q11 deletion

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9538314

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9538314

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth and development of the pulmonary vascular bed in patients with tetralogy of Fallot with or without pulmonary atresia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9538314

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/HRT.79.2.186

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

PMC publication ID

1728608

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

PubMed publication ID

9538314

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728608

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9538314%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

 

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