| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6220713 | The Journal of Pediatrics | 2014 | 8 Pages |
Abstract
Our data show a delay in the diagnosis of 22q11.2 deletion syndrome with noncardiac symptoms. This study provides guidelines for pediatricians and specialists for early identification of cases that can be confirmed by genetic testing, which would permit the provision of appropriate clinical management.
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Authors
Caterina MD, PhD, Pamela MD, Maria Cristina MD, Annarosa MD, Silvana MD, Roberto MD, Rita MD, Ezia Maria MD, Fabio MD, Andrea MD, PhD, Maria Luisa BSc, PhD, Baldassarre MD, Rosa MD, Veronica MD, Adriano MD, Fernando MD, Davide MD, Emilia MD, Paolo MD,