The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study

Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland

(2011) Anna Wozniak et al.   BMC Pediatrics

Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

(2011) Donna M. McDonald-McGinn et al.   MEDICINE

Children diagnosed with congenital cardiac malformations at the national university departments of pediatric cardiology: positive predictive values of data in the Danish National Patient Registry

(2011) Peter Agergaard et al.   Clinical Epidemiology

Cardiovascular Anomalies Associated With Chromosome 22q11.2 Deletion Syndrome

(2010) Kazuo Momma   AMERICAN JOURNAL OF CARDIOLOGY

Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India

(2010) Ashutosh Halder et al.   BMC Medical Genetics

Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review

(2010) Peter Agergaard et al.   European Journal of Medical Genetics

22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia

(2010) K. van Engelen et al.   HEART

Detecting 22q11.2 Deletions by Use of Multiplex Ligation-Dependent Probe Amplification on DNA from Neonatal Dried Blood Spot Samples

(2010) Karina M. Sørensen et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery

(2009) Yali Hu et al.   CARDIOLOGY IN THE YOUNG

Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patients

(2009) GM Repetto et al.   CLINICAL GENETICS

Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot

(2009) R. Rauch et al.   JOURNAL OF MEDICAL GENETICS

22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in Brazil

(2008) Rafael F.M. Rosa et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Chromosomal abnormalities among children born with conotruncal cardiac defects

(2008) Edward J. Lammer et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery

(2008) Lidia Ziolkowska et al.   EUROPEAN JOURNAL OF PEDIATRICS

Extracardiac features predicting 22q11.2 Deletion Syndrome in adult congenital heart disease

(2008) Wai Lun Alan Fung et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases

(2007) L. Gioli-Pereira et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY