(Q64975854)

English

Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival.

scientific article published in January 1984

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

tetralogy of Fallot

1 reference

based on heuristic

inferred from title

DiGeorge syndrome

1 reference

based on heuristic

inferred from title

author name string

W E Winter

1

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

J H Silverstein

2

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

D J Barrett

3

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

E Kiel

4

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

publication date

1 January 1984

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

141

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

3

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

171-172

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

https://scigraph.springernature.com/pub.10.1007/bf00443218

0 references

A deletion in chromosome 22 can cause DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital Cardiovascular Disease and Anomalies of the Third and Fourth Pharyngeal Pouch

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic hypoparathyroidism in two generations

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial thymic aplasia with intrauterine growth retardation and fetal death: a new syndrome or a variant of DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DiGeorge syndrome associated with multiple squamous cell carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial third and fourth pharyngeal pouch syndrome with truncus arteriosus: DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cardiomyopathy of hypoparathyroidism. Another reversible form of heart muscle disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic hypoparathyroidism in the newborn. Report of two cases born of diabetic mothers

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial thymic aplasia. Attempted reconstitution with fetal thymus in a Millipore diffusion chamber

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congestive heart failure secondary to idiopathic hypoparathyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic hypoparathyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/6698063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00443218

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2019

http://europepmc.org/abstract/MED/6698063

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