(Q35372597)

English

Spectrum of congenital heart defects and extracardiac malformations associated with chromosomal abnormalities: results of a seven year necropsy study

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Spectrum of congenital heart defects and extracardiac malformations associated with chromosomal abnormalities: results of a seven year necropsy study (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

congenital disorder

0 references

author name string

Tennstedt C

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Chaoui R

2

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Körner H

3

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Dietel M

4

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

language of work or name

0 references

publication date

1 July 1999

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

82

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

34-39

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Prenatal diagnosis of 22q11 deletions: a series of five cases with congenital heart defects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 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=1729082

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Genetic basis of DiGeorge and velocardiofacial syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 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=1729082

12 July 2018

Congenital Malformations in Autosomal Trisomy Syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Spectrum of congenital heart disease detected echocardiographically in prenatal life

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Congenital heart disease: prevalence at livebirth. The Baltimore-Washington Infant Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Distribution of congenital heart malformations in an autopsied child population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Cardiac and noncardiac malformations: observations in a population-based study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Congenital heart disease and extracardiac anomalies: associations and indications for fetal echocardiography

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Congenital heart defects in autopsy material from stillborn infants and children who died in the Central Bohemian Region from 1967--1976

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Extracardiac defects in children with congenital heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Extracardiac abnormalities in infants with congenital heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

12 July 2018

Some epidemiological aspects of congenital heart disease in Denmark

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

26 September 2018

Congenital heart disease in a cohort of 19,502 births with long-term follow-up

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1729082

26 September 2018

[Malformations of the heart and vascular system in autopsy material of children]

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

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/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The frequency of aneuploidy in prenatally diagnosed congenital heart disease: an indication for fetal karyotyping

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal anomalies in fetal congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Congenital heart disease found in autopsies from the University-Institute of Pathology in Leipzig (author's transl)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiovascular malformations associated with congenital anomalies of the urinary system. Observations in a series of 453 infants and children with urinary system malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prospective diagnosis of 1,006 consecutive cases of congenital heart disease in the fetus

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital Heart Disease in 56,109 Births Incidence and Natural History

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Genetics of hereditary cardiopathies]

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-cardiac malformations in individuals with outflow tract defects of the heart: the Baltimore-Washington Infant Study (1981-1989)

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiovascular abnormalities associated with congenital diaphragmatic hernia

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of congenital heart disease and fetal karyotyping

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal cytogenetic results from cases referred for 44 different types of abnormal ultrasound findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities of the heart and great arteries in first trimester chromosomally abnormal fetuses.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

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