Chromosomal abnormalities among children born with conotruncal cardiac defects (Q33797160)

29 July 2017

Chromosomal abnormalities among children born with conotruncal cardiac defects (English)

1 reference

29 July 2017

7

Suzan L Carmichael

1 reference

29 July 2017

8

Gary M Shaw

1 reference

29 July 2017

1

Edward J Lammer

1 reference

29 July 2017

3

David M Iovannisci

1 reference

29 July 2017

4

Kathleen Schultz

1 reference

29 July 2017

Jacqueline S Chak

2

1 reference

PubMed ID

19067405

29 July 2017

Kazutoyo Osoegawa

series ordinal

5

1 reference

PubMed ID

19067405

29 July 2017

Wei Yang

series ordinal

6

1 reference

29 July 2017

1 January 2009

1 reference

Birth Defects Research Part A: Clinical and Molecular Teratology

29 July 2017

1 reference

29 July 2017

85

1 reference

29 July 2017

30-35

1 reference

29 July 2017

1

1 reference

Reexpression of caveolin-1 in endothelium rescues the vascular, cardiac, and pulmonary defects in global caveolin-1 knockout mice

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pedia

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Klinefelter syndrome and other sex chromosomal aneuploidies

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

The incidence of congenital heart disease

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Left superior vena cava persistence in patients undergoing pacemaker or cardioverter-defibrillator implantation: a 10-year experience.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Jumonji, a nuclear protein that is necessary for normal heart development

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

jumonji gene is essential for the neurulation and cardiac development of mouse embryos with a C3H/He background

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Congenital heart disease in patients with Turner's syndrome. Italian Study Group for Turner Syndrome (ISGTS).

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Congenital heart disease in patients with Turner’s syndrome

4 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FBDRA.20541

Mechanisms of cardiac protection from ischemia/reperfusion injury: a role for caveolae and caveolin-1.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Rapid detection of the 22q11.2 deletion with quantitative real-time PCR.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Empiric recurrence risks in common and uncommon congenital heart lesions

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Cardiac malformations in relatives of children with truncus arteriosus or interruption of the aortic arch

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Caveolin-1 Null (−/−) Mice Show Dramatic Reductions in Life Span†

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2856481

Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching

30 October 2018

1 reference

12 December 2020

Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies

1 reference

12 December 2020

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

1 reference

12 December 2020

Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study

1 reference

12 December 2020

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

1 reference

12 December 2020

Deletion within chromosome 22 is common in patients with absent pulmonary valve syndrome

1 reference

12 December 2020

Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion

1 reference

12 December 2020

A genetic etiology for interruption of the aortic arch type B

1 reference

12 December 2020

Truncus arteriosus communis associated with chromosome 22q11 deletion

1 reference

12 December 2020

Frequency of 22q11 deletions in patients with conotruncal defects

1 reference

12 December 2020

Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies

1 reference

12 December 2020

Identifiers

DOI

10.1002/BDRA.20541

1 reference

29 July 2017

1 reference

29 July 2017

1 reference

PubMed ID

19067405