## Abstract ## BACKGROUND: The phenotype associated with deletion of the 22q11.2 chromosomal region is highly variable, yet little is known about the source of this variability. Cardiovascular anomalies, including tetralogy of Fallot, truncus arteriosus, interrupted aortic arch type B, perimembran
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome
β Scribed by Adriano Carotti; Maria Cristina Digilio; Gerardo Piacentini; Claudia Saffirio; Roberto M. Di Donato; Bruno Marino
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2008
- Tongue
- English
- Weight
- 136 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1940-5510
- DOI
- 10.1002/ddrr.6
No coin nor oath required. For personal study only.
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## Abstract The 22q11.2 deletion syndrome (22q11DS) is one of the most recognizable causes of congenital heart defects (CHDs), but the frequency varies in nonβselected populations. The purpose of this study was to determine the incidence and clinical features of patients with CHD and 22q11DS admitt
## Abstract There is an overwhelming evidence that children and adults with 22q11.2 deletion syndrome (22q11.2DS) have a characteristic behavioral phenotype. In particular, there is a growing body of evidence that indicates an unequivocal association between 22q11.2DS and schizophrenia, especially