Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease (Q35115372)

6 August 2017

Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease (English)

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6 August 2017

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4

Michael A Gatzoulis

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6 August 2017

Wai Lun Alan Fung

1

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6 August 2017

Eva W C Chow

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2

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6 August 2017

Gary D Webb

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3

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6 August 2017

Anne S Bassett

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5

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6 August 2017

11 January 2008

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International Journal of Cardiology

6 August 2017

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6 August 2017

131

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6 August 2017

1

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6 August 2017

51-58

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Tetralogy of Fallot: from fetus to adult

6 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Prenatally diagnosed pulmonary atresia with ventricular septal defect: echocardiography, genetics, associated anomalies and outcome.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Structural variation in the human genome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

22q11 deletion: a multisystem disorder requiring multidisciplinary input

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Challenges in the care of adult patients with congenital heart defects

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Patterns of dysmorphic features in schizophrenia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Genetic counselling for schizophrenia in the era of molecular genetics

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

22q11 deletion syndrome: a genetic subtype of schizophrenia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

22q11 deletion syndrome in adults with schizophrenia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Chromosome 22q11 microdeletions in tetralogy of Fallot

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Congenital heart disease in the general population: changing prevalence and age distribution.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Clinical features of 78 adults with 22q11 Deletion Syndrome.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Accuracy in identification of patients with 22q11.2 deletion by likely care providers using facial photographs.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Sensitivity and specificity of select biological indices in characterizing psychotic patients and their relatives.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Long-Term Outcome in Patients Undergoing Surgical Repair of Tetralogy of Fallot

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139626

Left superior vena cava in pediatric cardiology associated with extra-cardiac anomalies

16 November 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Tetralogy of Fallot associated with chromosome 22q11 deletion

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12 December 2020

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

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12 December 2020

Frequency of 22q11 deletions in patients with conotruncal defects

1 reference

12 December 2020

Guidelines for 22q11 deletion screening of patients with conotruncal defects

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12 December 2020

Frequent association of 22q11.2 deletion with tetralogy of Fallot

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12 December 2020

Anatomic patterns of conotruncal defects associated with deletion 22q11

1 reference

12 December 2020

Pulmonary atresia with ventricular septal defect: prevalence of deletion 22q11 in the different anatomic patterns

1 reference

12 December 2020

Cervical origin of the subclavian artery as a specific marker for monosomy 22q11

1 reference

12 December 2020

Delivery of care for adult patients with congenital heart disease in Europe: results from the Euro Heart Survey.

1 reference

12 December 2020

Cardiovascular anomalies associated with chromosome 22q11.2 deletion

1 reference

12 December 2020

10.1016/J.IJCARD.2007.08.141

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DOI

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6 August 2017

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6 August 2017

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