(Q43821719)

English

The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease

scientific article published in August 1996

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

author name string

K Devriendt

1

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

B Eyskens

2

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

A Swillen

3

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

M Dumoulin

4

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

M Gewillig

5

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

J P Fryns

6

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

publication date

1 August 1996

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

155

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

721

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8839734

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions within chromosome 22q11 in familial congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8839734

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions

1 reference

https://pubmed.ncbi.nlm.nih.gov/8839734

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prediction of persistent immunodeficiency in the DiGeorge anomaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/8839734

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8839734

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8839734

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/8839734

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S004310050477

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

ResearchGate publication ID

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