(Q54246365)

English

Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia.

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scholarly article

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia. (English)

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

tetralogy of Fallot

1 reference

based on heuristic

inferred from title

pulmonic stenosis

1 reference

based on heuristic

inferred from title

ventricular septal defect

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Bruno Dallapiccola

6

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

author name string

Digilio MC

1

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

Marino B

2

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

Grazioli S

3

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

Agostino D

4

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

Giannotti A

5

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

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publication date

1 June 1996

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

American Journal of Cardiology

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Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

77

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Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

15

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

1375-1376

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2896%2900212-3

7 January 2021

Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2896%2900212-3

7 January 2021

Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2896%2900212-3

7 January 2021

DiGeorge syndrome: part of CATCH 22.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2896%2900212-3

7 January 2021

Pulmonary atresia with ventricular septal defect. Selection of patients for systemic-to-pulmonary artery shunt based on echocardiography

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2896%2900212-3

7 January 2021

Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2896%2900212-3

7 January 2021

The gene for familial polyposis coli maps to the long arm of chromosome 5.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2896%2900212-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2896%2900212-3

7 January 2021

Identifiers

10.1016/S0002-9149(96)00212-3

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/8677886

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