(Q41912446)

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

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Europe PubMed Central

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10 November 2019

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

1 reference

Europe PubMed Central

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

10 November 2019

tetralogy of Fallot

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Stanislas Lyonnet

6

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10 November 2019

author name string

M Chessa

1

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10 November 2019

G Butera

2

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10 November 2019

P Bonhoeffer

3

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10 November 2019

L Iserin

4

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10 November 2019

J Kachaner

5

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10 November 2019

A Munnich

7

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10 November 2019

D Sidi

8

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10 November 2019

D Bonnet

9

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10 November 2019

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1 February 1998

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10 November 2019

1 reference

Europe PubMed Central

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10 November 2019

79

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10 November 2019

2

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10 November 2019

186-190

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10 November 2019

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

1 reference

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

5 June 2018

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

1 reference

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

5 June 2018

DiGeorge syndrome: part of CATCH 22.

1 reference

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

5 June 2018

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

1 reference

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

5 June 2018

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

1 reference

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

5 June 2018

Toward a molecular understanding of congenital heart disease

1 reference

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

5 June 2018

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

1 reference

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

5 June 2018

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

1 reference

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

5 June 2018

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

1 reference

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

5 June 2018

Neural crest cells contribute to normal aorticopulmonary septation

1 reference

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

5 June 2018

Mesenchymal derivatives from the neural crest

1 reference

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

5 June 2018

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

1 reference

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

5 June 2018

Dinucleotide repeat polymorphism at the D22S264 locus

1 reference

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

5 June 2018

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

1 reference

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

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.

1 reference

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

18 August 2018

Human haploinsufficiency — one for sorrow, two for joy

1 reference

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

2 December 2018

Microsatellite DNA markers detects 95% of chromosome 22q11 deletions

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac morphogenesis--recent research advances

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization

1 reference

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

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

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tetralogy of Fallot associated with chromosome 22q11 deletion

1 reference

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

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

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

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

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/HRT.79.2.186

1 reference

Europe PubMed Central

PMC publication ID

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

10 November 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

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

10 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

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

10 November 2019

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